https://jobboard.globalhealth.org Latest GHC Job Board Jobs Wed, 14 Jul 2021 04:49:41 Z https://jobboard.globalhealth.org/jobs/rss/15009536/research-regulatory-associate-sarcoma https://jobboard.globalhealth.org/jobs/rss/15009536/research-regulatory-associate-sarcoma New York, New York, At MSK, were running one of the largest clinical trials programs for cancer in the country, and at any time we are conducting hundreds of clinical trials to improve cancer care. We are seeking a Research Regulatory Associate (RRA) to join our Sarcoma service within the Department of Medicine. In this role, you will ensure the proper conduct of clinical research by developing, revising and maintaining accurate protocol tools at all times. You will: Work closely with management to assist in all aspects of regulatory oversight for trials in the service, from start-up through study closeout, and protocols in development. Assist in protocol submission, drafting of consents, reviewing protocol logistics. Assist in audits- reviewing and collecting regulatory documents. House all CVs, medical licenses, certifications and ensure they are current. Participate in special projects and task forces as determined by management. Utilize appropriate methodologies to collect patient/human subject information for a research project, database, and/or protocol. Generate reports to all necessary parties on the progress of the research project, database, or protocol, as needed. Assist in handling departmental data. Communicate with staff at all levels (principal investigators, clinical and research support staff). Ensure that all appropriate regulations are followed throughout the course of a research project, database, or protocol. Ensure that research protocols are approved by the Institutional Review Board and followed as written. Ensure that workflow is controlled and meets departmental needs. Manages ongoing departmental projects and crafts processes to ensure that goals are met. Participate or coordinate on both interdepartmental and intra-departmental organization-wide research projects as requested. Provide leadership, organizational, creative, or clerical support to established and new research initiatives. You Are: A good decision-maker, with proven success at making timely decisions that keep the organization moving forward. Able to hold yourself and others accountable in order to achieve goals and live up to commitments. Flexible in your approach and demeanor in order to align with the shifting demands of evolving circumstances. Knowledgeable of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA). You Have: A minimum of a High School Diploma with experience in clinical research or applicable experience. A Bachelors degree is preferred. At least 1 year of experience working in clinical research, preferably with experience in the regulatory space Note: There will be some weekend work expectations to cover potential Serious Adverse Events (SAE) reporting. Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15096051/clinical-research-supervisor-department-of-pediatrics-solid-tumor-ii https://jobboard.globalhealth.org/jobs/rss/15096051/clinical-research-supervisor-department-of-pediatrics-solid-tumor-ii New York, New York, We have an exciting opportunity to join our dynamic team in the Department of Pediatrics Solid Tumor II (STII) Division as Clinical Research Supervisor (CRS)! The STII Division encompasses General Oncology Sarcoma; and the Neuro-Oncology Service. As a CRS, you will supervise the day-to-day activities of Clinical Research Coordinators (CRCs) to ensure efficient and effective operations. You will be responsible for data management activities and for data integrity associated with clinical research. Also, you will have the opportunity to participate in special projects and task forces as determined by management. You will manage several research protocols, including investigator-initiated trials, industry-sponsored studies, as well as bio-specimen protocols. In the STII Division, our faculty regularly treat rare diseases and tumors on our robust portfolio of protocols. New drug development programs and treatment approaches are all part of the teams broad palette of expertise. What will you do: Staff Management and Development - Participate in the orientation, training and supervision of CRCs; participate in facilitating departmental trainings; align staff and resources with appropriate protocols and research needs; and maintain workflow consistency among staff with standardized processes. Operation Management - Ensure that workflow is managed and monitored to meet departmental and service needs; assist the Clinical Research Manager (CRM) with protocol activation, especially with start-up activities; monitor research portfolio for workload by appropriately managing and identifying service needs. Quality Assurance - Perform regular audits to ensure that the data collected is complete and accurate, and that the research project is carried out as planned. Regulatory Compliance - Ensure that all appropriate Institutional, State, and Federal regulations are followed throughout the course of a research project, database, or protocol. Ensure that research protocols are approved by the Institutional Review Board/Privacy Board (IRB/PB) and followed as written. Data collection - Utilize appropriate methodologies to collect patient/human subject information for research projects, databases, and/or protocols. Data reporting - Generate reports to all necessary parties. Prepare data for analysis, monitoring visits and audits. Clinical Research Billing Management - Implement Principal Investigator's decisions regarding Patient-Care Costs. Special Projects - Participate or coordinate on both interdepartmental and intra-departmental organization-wide research projects as requested. You will provide leadership, organizational, creative, or clerical support to established and new research initiatives. Who are you: Bachelor's degree with at least 3 years of clinical research experience OR a high school diploma with 6 years of clinical research experience Supervisory experience and experience with high volume trials is strongly preferred. Comprehensive knowledge and understanding of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA) is critical. Strong time management/project management skills. Knowledge of oncology-specific terminology is helpful. Experience in the use of various electronic data management systems. Strong Data management skills, including database design preferred. Basic knowledge of Microsoft suite (PowerPoint, Word, Access, Excel) and Teamshare. Effective at building formal and informal networks inside and outside the organization to further departmental and institutional goals. Adept at building partnerships and working collaboratively with others to meet shared objectives and goals. A good decision-maker, with shown success at making timely decisions that keep the organization moving forward. Eager to foster talent and support people in meeting their career goals and the organization's goals. Benefits Competitive compensation packages | Sick Time |Generous Vacation+ 12 holidays to recharge & refuel| Internal Career Mobility & Performance Consulting | Medical, Dental, Vision, FSA & Dependent Care|403b Retirement Savings Plan Match|Tuition Reimbursement |Parental Leave & Adoption Assistance |Commuter Spending Account |Fitness Discounts &Wellness Program | Resource Networks| Life Insurance & Disability | Remote Flexibility We believe in communication, openness, and thinking beyond your 8-hour day @ MSK. Its important to us that you have a sense of impact, community, and work/life balance to be and feel your best. #LI-POST Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15080247/car-t-data-research-project-associate-adult-bmt-service https://jobboard.globalhealth.org/jobs/rss/15080247/car-t-data-research-project-associate-adult-bmt-service New York, New York, At MSK, were running one of the largest clinical trials programs for cancer in the country, and at any time we are conducting hundreds of clinical trials to improve cancer care. We are seeking a Research Project Associate (RPA) to join our Adult Bone Marrow Transplant (ABMT) service within the Department of Medicine.In this role, you assist Principal Investigators (PIs) in analyzing and reporting data associated with retrospective and prospective research protocols. You will: Maintain a departmental database that houses data associated with patients receiving CAR-T therapy at MSKCC. Collaborate with internal and external investigators on ongoing data projects and data sharing initiatives while maintaining regulatory compliance. Participate in on-demand data abstraction from internal and external databases for IRB-approved research projects. Ensure data entered into departmental databases is QAed in a timely manner. If errors are identified, you will be responsible for developing corrective action plans to prevent recurrent errors. Participate in special projects and task forces as determined by management. Utilize appropriate methodologies to collect patient/human subject information for a research project, database, and/or protocol. Generate reports to all necessary parties on the progress of the research project, database, or protocol, as needed. Assist in handling departmental data. Communicate with staff at all levels (principal investigators, clinical and research support staff). Ensure that workflow is controlled and meets departmental needs. Manages ongoing departmental projects and crafts processes to ensure that goals are met. Participate or coordinate on both interdepartmental and intra-departmental organization-wide research projects as requested. Provide leadership, organizational, creative, or clerical support to established and new research initiatives. You Are: A good decision-maker, with proven success at making timely decisions that keep the organization moving forward. Able to hold yourself and others accountable in order to achieve goals and live up to commitments. Flexible in your approach and demeanor in order to align with the shifting demands of evolving circumstances. Knowledgeable of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA). You Have: A minimum of a High School Diploma with experience in clinical research or applicable experience. A Bachelors degree is preferred. At least 1 year of experience working in clinical research, preferably with experience indata entry across multiple databases. Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15074990/regulatory-research-associate-protocol-activation https://jobboard.globalhealth.org/jobs/rss/15074990/regulatory-research-associate-protocol-activation New York, New York, Regulatory Research Associate - Protocol Activation As an integral member of the research team and in compliance with all regulatory, institutional, and departmental requirements, the RRA performs all tasks associated with the regulatory management of research protocols within MSKCC. The RRA will be responsible for ensuring MSK is audit-ready at all times by maintaining up-to-date regulatory documents and regulatory files. The RRA also ensures the proper conduct of clinical research by developing, revising and maintaining accurate protocol tools at all times. You will: Perform regular audits to ensure that the data collected is complete and accurate and to ensure that the research project is completed as outlined. Work closely with management to assist in all aspects of regulatory oversight for trials in the service, from start-up through study closeout, and protocols in development. Will assist in protocol submission, drafting of consents, reviewing protocol logistics. Assist in protocol audits- reviewing and collecting regulatory documents, provide data entry assistance if needed. House all CVs, medical licenses, certifications and ensure they are current. Participate in special projects and task forces as determined by management. Utilize appropriate methodologies to collect patient/human subject information for a research project, database, and/or protocol. Generate reports to all necessary parties on the progress of the research project, database, or protocol, as needed. Assist in handling departmental data. Communicate with staff at all levels (principal investigators, clinical and research support staff). Ensure that all appropriate Institutional, State, and Federal regulations are followed throughout the course of a research project, database, or protocol. Ensures that research protocols are approved by the Institutional Review Board and followed as written. Ensure that workflow is controlled and meets departmental needs. Manages ongoing departmental projects and crafts processes to ensure that goals are met. Participate or coordinate on both interdepartmental and intra-departmental organization-wide research projects as requested. Provide leadership, organizational, creative, or clerical support to established and new research initiatives. You need: A minimum of a High School Diploma with experience in clinical research or applicable experience. A Bachelors degree is preferred. Must be able to work independently, be flexible, and meet tight deadlines. Microsoft applications, database knowledge a plus. Must have a comprehensive knowledge and understanding of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA). Hours: Monday - Friday, 9 am - 5 pm Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15057291/research-regulatory-associate-thoracic-medicine https://jobboard.globalhealth.org/jobs/rss/15057291/research-regulatory-associate-thoracic-medicine New York, New York, Regulatory Research Associate- Thoracic Medicine As an integral member of the research team and in compliance with all regulatory, institutional, and departmental requirements, the RRA performs all tasks associated with the regulatory management of research protocols within MSKCC. The RRA will be responsible for ensuring MSK is audit-ready at all times by maintaining up-to-date regulatory documents and regulatory files. The RRA also ensures the accurate conduct of clinical research by developing, revising and maintaining accurate protocol. You will: Perform regular audits to ensure that the data collected is complete and accurate and to ensure that the research project is completed as outlined. Work closely with management to assist with all of the regulatory oversight for clinical trials in the service, from start-up through study closeout, and protocols in development. Will assist with protocol submission, drafting of consents, reviewing protocol logistics. Assist in protocol audits- reviewing and collecting regulatory documents, provide data entry assistance if needed. House all CVs, medical licenses, certifications and ensure they are current. Participate in special projects and task forces as determined by management. Utilize appropriate methodologies to collect patient/human subject information for a research project, database, and/or protocol. Generate reports to all vital parties on the progress of the research project, database, or protocol, as needed. Assist in handling departmental data. Connect with staff at all levels (principal investigators, clinical and research support staff). Have worked with principal investigators. Ensure that all appropriate Institutional, State, and Federal regulations are followed throughout the course of a research project, database, or protocol. Ensures that research protocols are approved by the Institutional Review Board (IRB) and followed as written. Ensure that workflow is controlled and meets departmental needs. Leads ongoing departmental projects and crafts processes to ensure that goals are met. Participate or coordinate on both interdepartmental and intra-departmental organization-wide research projects as requested. Provide leadership, organizational, creative, or clerical support to established and new research initiatives. You need: A minimum of a High School Diploma with experience at least 1 year of clinical research or applicable experience. A Bachelors degree is preferred. An ability to work independently, be flexible, and meet tight deadlines. Microsoft applications, database knowledge a plus. Must have an extensive knowledge and understanding of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA). Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15036961/research-regulatory-associate-gmo-women-s-health https://jobboard.globalhealth.org/jobs/rss/15036961/research-regulatory-associate-gmo-women-s-health New York, New York, Regulatory Research Associate- GMO-Women's Health As an integral member of the research team and in compliance with all regulatory, institutional, and departmental requirements, the RRA performs all tasks associated with the regulatory management of research protocols within MSKCC. The RRA will be responsible for ensuring MSK is audit-ready at all times by maintaining up-to-date regulatory documents and regulatory files. The RRA also ensures the proper conduct of clinical research by developing, revising and maintaining accurate protocol tools at all times. You will: Perform regular audits to ensure that the data collected is complete and accurate and to ensure that the research project is completed as outlined. Work closely with management to assist in all aspects of regulatory oversight for trials in the service, from start-up through study closeout, and protocols in development. Will assist in protocol submission, drafting of consents, reviewing protocol logistics. Assist in protocol audits- reviewing and collecting regulatory documents, provide data entry assistance if needed. House all CVs, medical licenses, certifications and ensure they are current. Participate in special projects and task forces as determined by management. Utilize appropriate methodologies to collect patient/human subject information for a research project, database, and/or protocol. Generate reports to all necessary parties on the progress of the research project, database, or protocol, as needed. Assist in handling departmental data. Communicate with staff at all levels (principal investigators, clinical and research support staff). Ensure that all appropriate Institutional, State, and Federal regulations are followed throughout the course of a research project, database, or protocol. Ensures that research protocols are approved by the Institutional Review Board and followed as written. Ensure that workflow is controlled and meets departmental needs. Manages ongoing departmental projects and crafts processes to ensure that goals are met. Participate or coordinate on both interdepartmental and intra-departmental organization-wide research projects as requested. Provide leadership, organizational, creative, or clerical support to established and new research initiatives. You need: A minimum of a High School Diploma with experience in clinical research or applicable experience. A Bachelors degree is preferred. Must be able to work independently, be flexible, and meet tight deadlines. Microsoft applications, database knowledge a plus. Must have a comprehensive knowledge and understanding of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA). Hours: Monday - Friday, 9 AM - 5 PM Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15032086/regulatory-research-associate-pediatrics https://jobboard.globalhealth.org/jobs/rss/15032086/regulatory-research-associate-pediatrics New York, New York, Regulatory Research Associate- Pediatrics As an integral member of the research team and in compliance with all regulatory, institutional, and departmental requirements, the RRA performs all tasks associated with the regulatory management of research protocols within MSKCC. The RRA will be responsible for ensuring MSK is audit-ready at all times by maintaining up-to-date regulatory documents and regulatory files. The RRA also ensures the proper conduct of clinical research by developing, revising and maintaining accurate protocol tools at all times. You will: Perform regular audits to ensure that the data collected is complete and accurate and to ensure that the research project is completed as outlined. Work closely with management to assist in all aspects of regulatory oversight for trials in the service, from start-up through study closeout, and protocols in development. Will assist in protocol submission, drafting of consents, reviewing protocol logistics. Assist in protocol audits- reviewing and collecting regulatory documents, provide data entry assistance if needed. House all CVs, medical licenses, certifications and ensure they are current. Participate in special projects and task forces as determined by management. Utilize appropriate methodologies to collect patient/human subject information for a research project, database, and/or protocol. Generate reports to all necessary parties on the progress of the research project, database, or protocol, as needed. Assist in handling departmental data. Communicate with staff at all levels (principal investigators, clinical and research support staff). Ensure that all appropriate Institutional, State, and Federal regulations are followed throughout the course of a research project, database, or protocol. Ensures that research protocols are approved by the Institutional Review Board and followed as written. Ensure that workflow is controlled and meets departmental needs. Manages ongoing departmental projects and crafts processes to ensure that goals are met. Participate or coordinate on both interdepartmental and intra-departmental organization-wide research projects as requested. Provide leadership, organizational, creative, or clerical support to established and new research initiatives. You need: A minimum of a High School Diploma with experience in clinical research or applicable experience. A Bachelors degree is preferred. Must be able to work independently, be flexible, and meet tight deadlines. Microsoft applications, database knowledge a plus. Must have a comprehensive knowledge and understanding of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA). Hours: Monday - Friday, 9 am - 5 pm Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15118368/research-project-associate-radiology-tumor-response-assessment-program https://jobboard.globalhealth.org/jobs/rss/15118368/research-project-associate-radiology-tumor-response-assessment-program New York, New York, As a Research Project Associate (RPA) in the Department of Radiologys Tumor Response Assessment Program, you willsupports Oncologist, Radiologists, and Clinical Research Support Staff to assess how clinical research participants respond to a therapeutic drug. These assessments help determine whether a clinical research participant has improved, stayed the same, or worsened while receiving a therapeutic drug. As member of the tumor response assessment team, you will manage operations and coordinate the rollout of strategic projects that affect therapeutic clinical research trials. One major initiative we are rolling out at MSK is to use an electronic solution for completing these assessments. The application we utilize supports several hundred open clinical trials across MSK and promotes a standardized workflow that is compliant with regulatory requirements. Our team manages all aspects of this initiative, from coordinating and conducting in-service meetings to introduce the application, trial setup, assisting with training/education critical staff, maintaining day to day operations, and providing technical support to end users amongst other tasks. Additionally, as an integral member of the team, you will be involved in developing and implementing new initiatives that will directly impact clinical research trials within and across departments at MSK. You will: Participate in special projects and task forces as determined by management. Utilize appropriate methodologies to collect patient information Generate reports to all necessary parties on the progress Assist with high-level departmental projects requiring data management support; provide data entry solutions as needed. Perform regular audits to ensure that the platform is functioning and to ensure that the research requests are carried out as outlined. Ensure that workflow is controlled and meets departmental needs. Manages ongoing departmental projects and creates processes to ensure that goals are met. Participate or coordinate on both interdepartmental and intradepartmental organization-wide research projects as requested. Provide leadership, organizational, creative, or clerical support to established and new research initiatives. You Are: Able to operate effectively, even when things are not clear or the way forward is not obvious. Adept at planning and prioritizing work to meet commitments aligned with organizational goals. Action-oriented and eager to embrace new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm. You Have: A High School Diploma/GED with experience in clinical research or applicable experience. At least 2 years of clinical research experience Bachelor's degree preferred Project management experience is a plus Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/14997889/clinical-research-project-manager-gi-research https://jobboard.globalhealth.org/jobs/rss/14997889/clinical-research-project-manager-gi-research New York, New York, Memorial Sloan Kettering Cancer Center is seeking a Research Project Manager for the Gastrointestinal Medical Oncology Service. The Research Project Manager is responsible for a variety of clinical research projects both prospective and retrospective in nature. Commitment to accuracy, high attention-to-detail, and ability to work independently are critical competencies for the role. You will: Manage the functions and activities of assigned projects within the research organization, specifically overseeing the clinic initiatives and staff. Serve as the primary liaison for all research clinic activities at 53rd street Play a key role in the submission of patient reimbursements for clinical trials Assist with high level department projects requiring clinic support. Extract, compile, and analyze data to generate reports for leadership. Participate in special projects and task forces as determined by management. Support the work of investigators to accomplish research goals. Provide oversight and support to five to seven clinical specialists (CRSps) Have in-depth knowledge of the processes/procedures associated with clinical practice, clinical research and/or a strong information systems expertise in the latest technologies. You need: A Bachelors degree with at least 3-4 years of experience in clinical research and/or other applicable research investigation OR a high school diploma with 7 years of clinical experience. Knowledge in clinical trial regulatory and safety management preferred. Masters degree preferred. Ability to solve problems by using a logical, systematic, sequential approach. Excellent interpersonal, verbal and written communication skills. Strong organizational, prioritization, and project management skills. Proven ability to manage clinical research projects with strict deadlines. Must have a comprehensive knowledge and understanding of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA). Benefits Competitive compensation packages | Sick Time |Generous Vacation+ 12 holidays to recharge & refuel| Internal Career Mobility & Performance Consulting | Medical, Dental, Vision, FSA & Dependent Care|403b Retirement Savings Plan Match|Tuition Reimbursement |Parental Leave & Adoption Assistance |Commuter Spending Account |Fitness Discounts &Wellness Program | Resource Networks| Life Insurance & Disability | Remote Flexibility We believe in communication, openness, and thinking beyond your 8-hour day @ MSK. Its important to us that you have a sense of impact, community, and work/life balance to be and feel your best. #LI-POST Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15066055/research-regulatory-associate-multiple-myeloma https://jobboard.globalhealth.org/jobs/rss/15066055/research-regulatory-associate-multiple-myeloma New York, New York, At MSK, were running one of the largest clinical trials programs for cancer in the country, and at any time we are conducting hundreds of clinical trials to improve cancer care. We are seeking a Research Regulatory Associate (RRA) to join our Multiple Myeloma service within the Department of Medicine. In this role, you will ensure the proper conduct of clinical research by developing, revising and maintaining accurate protocol tools at all times. You will: Work closely with management to assist in all aspects of regulatory oversight for trials in the service, from start-up through study closeout, and protocols in development. Assist in protocol submission, drafting of consents, reviewing protocol logistics. Assist in audits- reviewing and collecting regulatory documents. House all CVs, medical licenses, certifications and ensure they are current. Participate in special projects and task forces as determined by management. Utilize appropriate methodologies to collect patient/human subject information for a research project, database, and/or protocol. Generate reports to all necessary parties on the progress of the research project, database, or protocol, as needed. Ensure that all appropriate regulations are followed throughout the course of a research project, database, or protocol. Ensure that research protocols are approved by the Institutional Review Board and followed as written. Ensure that workflow is controlled and meets departmental needs. Manages ongoing departmental projects and crafts processes to ensure that goals are met. Participate or coordinate on both interdepartmental and intra-departmental organization-wide research projects as requested. Provide leadership, organizational, creative, or clerical support to established and new research initiatives. You Are: A good decision-maker, with proven success at making timely decisions that keep the organization moving forward. Able to hold yourself and others accountable in order to achieve goals and live up to commitments. Flexible in your approach and demeanor in order to align with the shifting demands of evolving circumstances. Knowledgeable of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA). You Have: A minimum of a High School Diploma with experience in clinical research or applicable experience. A Bachelors degree is preferred. At least 1 year of experience working in clinical research, preferably with experience in the regulatory space Note: There will be some weekend work expectations to cover potential Serious Adverse Events (SAE) reporting. Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15118397/research-project-associate-behavioral-sciences-u01-grant https://jobboard.globalhealth.org/jobs/rss/15118397/research-project-associate-behavioral-sciences-u01-grant New York, New York, We are seeking a Research Project Associate to manage our five-year research project sought at developing and evaluating informative materials about genetic testing for cancer patients who speak different languages and have diverse cultural and educational backgrounds. Opportunities exist for research and academic professional development. This position is currently funded full-time for five years. This position requires literacy of Haitian Creole and/or Spanish. You will: Be responsible for management of all components of this project, including database development and maintenance, data collection and entry, communicating progress and challenges, management of vendor/collaborator relationships, and working with the study team and principal investigator (PI; Jada Hamilton, PhD, MPH) to handle and analyze the study data. Support the PI and study team as needed for data management and relevant project duties for the Behavioral Sciences and Psychology service Provide regular reports to the PI regarding study progress and challenges and work with the PI to address any problems that arise; Coordinate and participate in weekly study meetings Design database(s) and tools to facilitate data collection as needed for assigned research projects; Maintain study databases, codebooks, and procedures for data entry and monitoring Acquire informed consent and coordinate questionnaires and qualitative interviews when vital Ensure coordination and implementation of project-related activities; Assist in the preparation of grants, presentations, and manuscripts; Perform literature searches Have other tasks as needed You Are: Able to work independently as well as manage a team Able to prioritize and schedule work activities to ensure that workflow is efficient and meets the needs of the project Able to work independently and within a large team setting You Need: Minimum of 2 years of relevant research experience (1 year if you have a Masters degree) Masters degree (e.g., public health, implementation science or related field) preferred Language requirement Spanish and/or Haitian Creole Fluency Excellent knowledge of Microsoft Office, Excel, Access, and SPSS (or SAS, SQL) Excellent knowledge of REDCap preferred Knowledge of Visio and/or Gant project management software is helpful Background knowledge in genetics and genetic counseling is welcome but not required Excellent data management, organizational, oral and written communication, project coordination and interpersonal skills. Outstanding judgment, initiative, and attention to detail #LI-POST Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/14985720/research-project-manager-adult-bone-marrow-transplant https://jobboard.globalhealth.org/jobs/rss/14985720/research-project-manager-adult-bone-marrow-transplant New York, New York, We are seeking a Research Project Manager (RPM) to join the Adult Bone Marrow Transplant service, focusing on their GVHD protocols. You Will: Supervise day to day activities of one Clinical Research Coordinator and one Clinical Research Associate Manage the functions and activities of assigned GVHD projects within the research organization. Oversee chart reviews Manage the data management team to ensure accountability and quality of data. Manage a quality assurance program by reviewing data of research for accuracy and compliance. Support the work of Attendings, fellows and research assistants to accomplish research goals. Work on departmental initiatives relating to clinical research data management, specifically database management to ensure the highest quality data for the clinical research programs. You Are: Able to hold yourself and others accountable in order to achieve goals and live up to commitments. An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding. Able to operate effectively, even when things are not clear or the way forward is not obvious You Have: A Bachelors degree with at least 4-7 years of experience in clinical research, preferably in Hem Onc Ability to solve problems by using a logical, systematic, sequential approach. Strong organizational, prioritization, and project management skills. Proven ability to manage clinical research projects with strict deadlines. Must have a comprehensive knowledge and understanding of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA). Experience working with breast cancer data/or large scale registry projects is a plus. Benefits Competitive compensation packages | Sick Time |Generous Vacation+ 12 holidays to recharge & refuel| Internal Career Mobility & Performance Consulting | Medical, Dental, Vision, FSA & Dependent Care|403b Retirement Savings Plan Match|Tuition Reimbursement |Parental Leave & Adoption Assistance |Commuter Spending Account |Fitness Discounts &Wellness Program | Resource Networks| Life Insurance & Disability | Remote Flexibility We believe in communication, openness, and thinking beyond your 8-hour day @ MSK. Its important to us that you have a sense of impact, community, and work/life balance to be and feel your best. #LI-POST Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15118401/research-project-associate-cancer-health-equity-research-program https://jobboard.globalhealth.org/jobs/rss/15118401/research-project-associate-cancer-health-equity-research-program New York, New York, Are you passionate about cancer health disparities? We are hiring for a Research Project Associate (RPA) to join our dynamic Cancer Health Equity Research Program (CHERP). In CHERP, our mission is to decrease cancer health disparities experienced by certain racial, ethnic and low-socioeconomic populations by expanding their access to clinical trials. We have agreements with several local community hospitals, which allows us to open MSK studies with our partner sites. These partnerships allow us to offer some of MSK's cutting-edge cancer clinical trials to a broader, more diverse patient population. In this role, you will work on-site at the Queens Hospital Center in Jamaica, Queens, serving as a liaison between the site and MSK. You will provide data management and regulatory support for open studies at the site. Also, you will have on site management of day to day protocol operations. You will: Perform data management activities and for data accuracy and integrity associated with clinical research within the disease management team and/or service specific level. Be responsible for protocol submission, drafting site consents, reviewing protocol logistics. Facilitate in navigating CHERP site patients to MSK clinical trials at main campus. Participate in special projects and task forces as determined by management. Utilize appropriate methodologies to collect patient/human subject information for a research project, database, and/or protocol. Generate reports to all necessary parties on the progress of the research project, database, or protocol. Communicate with staff at all levels (principal investigators, clinical and research support staff). Perform regular audits to ensure that the data collected is complete and accurate and that research project was carried out as outlined. Be responsible for regulatory compliance and ensures that all appropriate Institutional, State, and Federal regulations are followed. Ensure that research protocols are approved by the Institutional Review Board and followed as written. Ensure that workflow is controlled and meets department needs. Manages ongoing departmental projects and creates processes to ensure that goals are met. Participate or coordinate on both inter-institutional and intra-institutional organization-wide research projects as requested. Provide leadership, organizational, creative, or clerical support to established and new research initiatives. You Are: Action-oriented and eager to embrace new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm. Able to hold yourself and others accountable in order to achieve goals and live up to commitments. An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding. You need: With Bachelor's, at least 1 year of clinical research in oncology, or as determined by hiring manager. A minimum of a High School Diploma with at least 3-4 years of clinical research experience Must be able to work independently, be flexible, and meet tight deadlines. Microsoft applications, database knowledge a plus. Experience or interest in health disparities Must have a comprehensive knowledge and understanding of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA). Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15118384/research-regulatory-associate-gu-prostate-service https://jobboard.globalhealth.org/jobs/rss/15118384/research-regulatory-associate-gu-prostate-service New York, New York, At MSK, were running one of the largest clinical trials programs for cancer in the country, and at any time we are conducting hundreds of clinical trials to improve cancer care. We have a Research Regulatory Associate (RRA) opportunity in our Genitourinary(GU) Prostate Service for the Department of Medicine . As an integral member of the research team, you will perform all tasks associated with the regulatory management of research protocols within MSKCC. The RRA will be responsible for ensuring MSK is audit ready at all times by maintaining up-to-date regulatory documents and regulatory files. The RRA also ensures the proper conduct of clinical research by developing, revising and maintaining accurate protocol tools at all times. You will: Work closely with management to assist in all aspects of regulatory oversight for trials in the service, from start-up through study closeout, and protocols in development. Assist in protocol submission, drafting of consents, reviewing protocol logistics. Assist in all regulatory related IRB submissions for the lifetime of a protocol (continuing review reports, amendments, etc). Assist in audits- reviewing and collecting regulatory documents. House all CVs, medical licenses, certifications and ensure they are current. Participate in special projects and task forces as determined by management. Utilize appropriate methodologies to collect patient/human subject information for a research project, database, and/or protocol. Generate reports to all necessary parties on the progress of the research project, database, or protocol, as needed. Assist in handling departmental data. Communicate with staff at all levels (principal investigators, clinical and research support staff). Ensure that all appropriate regulations are followed throughout the course of a research project, database, or protocol. Ensure that research protocols are approved by the Institutional Review Board and followed as written. Ensure that workflow is controlled and meets departmental needs. Manages ongoing departmental projects and crafts processes to ensure that goals are met. Participate or coordinate on both interdepartmental and intra-departmental organization-wide research projects as requested. Provide leadership, organizational, creative, or clerical support to established and new research initiatives. You Are: A good decision-maker, with proven success at making timely decisions that keep the organization moving forward. Able to hold yourself and others accountable in order to achieve goals and live up to commitments. Proven success in tasks that require attention to detail. A strong communicator, understanding the importance of providing stakeholders with relevant updates including notification of completed action items. Flexible in your approach and demeanor in order to align with the shifting demands of evolving circumstances. Knowledgeable of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA). You Have: A minimum of a High School Diploma with experience in clinical research or applicable experience. A Bachelors degree is preferred. At least 1 year of experience working in clinical research, preferably with experience in the regulatory space Hours: Monday - Friday, 9 AM - 5 PM There will be some weekend work expectations to cover potential Serious Adverse Events (SAE) reporting. Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15021482/regulatory-research-associate-early-drug-development https://jobboard.globalhealth.org/jobs/rss/15021482/regulatory-research-associate-early-drug-development New York, New York, At MSK, were running one of the largest clinical trials programs for cancer in the country, and at any time we are conducting hundreds of clinical trials to improve cancer care. We have a Research Regulatory Associate (RRA) opportunity with our Early Drug Development Service in the Department of Medicine . As an integral member of the research team, you will perform all tasks associated with the regulatory management of research protocols within MSKCC. In this role, you will be responsible for ensuring we are audit ready at all times by maintaining up-to-date regulatory documents and regulatory files. You will also ensure the proper conduct of clinical research by developing, revising and maintaining accurate protocol tools at all times. You will: Work closely with management to assist in all aspects of regulatory oversight for trials in the service, from start-up through study closeout, and protocols in development. Assist in protocol submission, drafting of consents, reviewing protocol logistics. Assist in audits- reviewing and collecting regulatory documents. House all CVs, medical licenses, certifications and ensure they are current. Participate in special projects and task forces as determined by management. Utilize appropriate methodologies to collect patient/human subject information for a research project, database, and/or protocol. Generate reports to all necessary parties on the progress of the research project, database, or protocol, as needed. Assist in handling departmental data. Communicate with staff at all levels (principal investigators, clinical and research support staff). Ensure that all appropriate regulations are followed throughout the course of a research project, database, or protocol. Ensure that research protocols are approved by the Institutional Review Board and followed as written. Ensure that workflow is controlled and meets departmental needs. Manages ongoing departmental projects and crafts processes to ensure that goals are met. Participate or coordinate on both interdepartmental and intra-departmental organization-wide research projects as requested. Provide leadership, organizational, creative, or clerical support to established and new research initiatives. You Are: A good decision-maker, with proven success at making timely decisions that keep the organization moving forward. Able to hold yourself and others accountable in order to achieve goals and live up to commitments. Flexible in your approach and demeanor in order to align with the shifting demands of evolving circumstances. Knowledgeable of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA). You Have: A minimum of a High School Diploma with experience in clinical research or applicable experience. A Bachelors degree is preferred. At least 2 years of experience working in clinical research, preferably with experience in the regulatory space Hours : Monday - Friday, 9 AM - 5 PM. 37.5 hours per week. There will be some weekend work expectations to cover potential Serious Adverse Events (SAE) reporting. Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15114433/research-project-manger-biomarker-development-program https://jobboard.globalhealth.org/jobs/rss/15114433/research-project-manger-biomarker-development-program New York, New York, Memorial Sloan Kettering Cancer Center is seeking a Research Project Manager for the Biomarker Development Program (BDP). The Research Project Manager is responsible for a variety of clinical research projects both prospective and retrospective in nature. Commitment to accuracy, high attention-to-detail, and ability to work independently are critical competencies for the role. You will: Manages program data. Communicates with all levels of staff (Principal Investigators (PI), clinical and research support staff) to determine database needs and performs analysis as necessary. Serves as the primary contact for all levels of staff regarding data administration matters as they relate to the service and protocol databases. This includes the review of standards with staff, identification of deficits, and participating in resolving problems. Prospectively communicate and enforce standards, create new initiatives, and create and oversee all staff education on data management. Serve as the primary contact with PIs, other institutions, services/departments, clinical and research fellows on all data related questions. Set standards and enforce data management practices within the program. Determines data management issues and resolves problems immediately or tracks problems until they are resolved. Analyzes departmental database needs and proposes and implements recommendations/ solutions to respond to those needs. Designs and builds databases to address changing needs inside and outside of the institution. Proficiently uses research databases (e.g., CRDB, DMS/HIS, Access, Excel, Case Report Forms, Caisis) to complete assigned tasks or to assist research staff. As needed, enters and tracks data in the relevant data collection form (e.g., CRDB, DMS/HIS, various PC-based systems, Case Report Forms, Access, Caisis) as per established protocol or project timelines. Participate in special projects and task forces as determined by management. Support the work of investigators to accomplish research goals. Have in-depth knowledge of the processes/procedures associated with clinical practice, clinical research and/or a strong information systems expertise in the latest technologies. You need: A Bachelors degree with at least 4 years of experience in clinical research and/or other applicable research investigation OR a high school diploma with 7 years of clinical experience. Knowledge in clinical trial regulatory and safety management preferred. Masters degree preferred. Masters in biostatistics a plus. Experience with Microsoft Office including Excel and Access, database knowledge. Experience with basic SPSS required and platforms like STATA and R a plus. Knowledge of human anatomy and physiology required. Ability to solve problems by using a logical, systematic, sequential approach. Excellent interpersonal, verbal and written communication skills. Strong organizational, prioritization, and project management skills. Proven ability to manage clinical research projects with strict deadlines. Must have a comprehensive knowledge and understanding of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA). Benefits Competitive compensation packages | Sick Time |Generous Vacation+ 12 holidays to recharge & refuel| Internal Career Mobility & Performance Consulting | Medical, Dental, Vision, FSA & Dependent Care|403b Retirement Savings Plan Match|Tuition Reimbursement |Parental Leave & Adoption Assistance |Commuter Spending Account |Fitness Discounts &Wellness Program | Resource Networks| Life Insurance & Disability | Remote Flexibility We believe in communication, openness, and thinking beyond your 8-hour day @ MSK. Its important to us that you have a sense of impact, community, and work/life balance to be and feel your best. #LI-POST Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15084787/program-administrator-bone-marrow-transplant-program https://jobboard.globalhealth.org/jobs/rss/15084787/program-administrator-bone-marrow-transplant-program Rochester, New York, Program Administrator, Bone Marrow Transplant Program Job ID: 229661 Location: Strong Memorial Hospital Full/Part Time: Full-Time Regular/Temporary: Regular Opening Full Time 40 hours Grade 057 Cancer Center SMH Schedule 8 AM-4:30 PM Responsibilities GENERAL PURPOSE: Responsible for the administrative, operational and financial management of the Transplant and Cellular Therapy Program at URMC. Accountable for carrying out the tri-fold mission of the Medical Center services through successful development of strategic plans, business and operational plans for new and/or expansion of services, facility and capital planning, organizational operating budget and expense management, facility and equipment expansion projects, marketing, web and fundraising proposals. Under the direction of Transplant and Cellular Therapy Program Director and the Senior Program Administrator for the Wilmot Cancer Institute, serves as the principal administrator for carrying out the missions of the Transplant and Cellular Therapy Program. This position interfaces on a daily basis with the BMT Clinical Director, Immune Effector Cell Therapy Director, and other key providers, working closely with the Department of Medicine and WCI leadership. RESPONSIBILITIES: Strategic Initiatives Works collaboratively with Medical Center Senior Leadership team and WCI leadership to develop and implement department strategic initiatives including: new programs and program expansions; program innovations such as regional expansion opportunities; digital health and special populations; capital infrastructure development; network and payer relationships; innovative academic programs needing faculty; and fellow recruitments. Operations Management Oversees operational functions to ensure clinical and academic programs have the appropriate infrastructure to support excellence in teaching, research and clinical care delivery. This would include: inpatient and outpatient program operations; decision support reporting; departmental reputation building and branding (web, marketing, PR, US News and World Report and advancement proposals); quality infrastructure development; service-line liaison to all extramural agencies and officials; primary liaison to all community-based collaborations; and planning and implementation of major clinical, research and teaching initiatives. Plans for and directs the administrative support staff for all clinical, research and educational program activities to assure efficient and effective use of resources. Establishes internal program policies and procedures, assuring compliance with the University and Medical Center requirements. Represents the Hospital, Wilmot Cancer Institute and the Transplant and Cellular Therapy Program at local and national forums on transplant and cellular therapy services. Actively participates in Local, State and National organizations associated with the provision of transplant and cellular therapy services including ASTCT. Responsible for operations, infrastructure, program management functions, quality assurance and improvement programs, revenue cycle management, compliance with regulatory standards, clinical trials administration, and adherence to all regulatory policies and procedures (FACT, FDA, CMS, JCAHO, NYSDOH). Maintains a liaison role with various Medical Center and University ancillary and support services for the purpose of information sharing, interdepartmental planning and administrative matters. Responsible for the oversight of all resources and processes required for successful maintenance of all data systems related to transplant and cellular therapy services, including CIBMTR. Assures compliance with University policy and procedures, Department of Medicine, JCAHO, FACT, CIBMTR, professional licensing and certification boards, federal regulatory agencies and NYS transplant and cellular therapy organizations. Finance Serves as the Transplant and Cellular Therapy Program financial officer responsible for program capital and operating budgets, assuring fiscal control through a reliable system of expenditure and revenue accounting. Works with Managed Care Services to develop and respond to insurance company RFPs, organizes site visits and help to set financial criteria for global pricing. Coordinates with WCI and the Medical Center planning office on the development of all CONs required for new or expanding programs. Monitors contract performance and oversees program expansion projects and budgets. Oversees preparation of operating and capital budgets; faculty compensation plans; prepares business plans for incremental resources and program expansions; supervises the coordination and review of quarterly reports to leadership including inpatient, outpatient, research and contract service performance. Directs analysis and report preparation of strategic initiative performance, service trends and other projections, revenue and expenses generated from services, grants and other academic programs. Leadership Fosters effective communication with employees, peers, and leaders; builds and maintains relationships; develops others; and manages projects, team and work groups. In partnership with Department leaders and the HR Business Partner, oversees departmental human resources functions regarding structure, employment, compensation review, promotions, disciplinary actions and terminations. Monitors staff engagement and initiates actions to ensure high levels of engagement. Articulates goals and coaches staff for optimal performance toward stated goals. Establishes a service culture to provide a first rate experience for customers (patients, referring providers, faculty). Ensures staff are provided job training and professional development, performance evaluations, coaching. Manages change process; models Org values; solves problems; makes effective decisions using data/input from stakeholders. Exhibits service oriented behavior, responsible for service improvement leadership in the division. Models Strong Commitment behaviors and encourages staff to follow by example. Ensures that senior leadership goals and hospital strategic plan is communicated to staff and physicians Other duties as assigned QUALIFICATIONS Graduate degree, preferably in Health Administration or Business Administration required 3-5 years of relevant experience in personnel, fiscal and resource management required Or an equivalent combination of education and experience required. How To Apply All applicants must apply online. EOE Minorities/Females/Protected Veterans/Disabled To apply, visit https://ps.its.rochester.edu/psp/PSApplyOnline/EMPLOYEE/HRMS/c/HRS_HRAM_FL.HRS_CG_SEARCH_FL.GBL?Page=HRS_APP_JBPST_FL&Action=U&FOCUS=Applicant&SiteId=1&JobOpeningId=229661&PostingSeq=1 Copyright ©2017 Jobelephant.com Inc. All rights reserved. Posted by the FREE value-added recruitment advertising agency jeid-8f0ee0667ca7bd4b947c2746e04c5480 Thu, 08 Jul 2021 12:22:37 -0400 https://jobboard.globalhealth.org/jobs/rss/15118398/research-and-residency-position-in-therapeutic-medical-physics https://jobboard.globalhealth.org/jobs/rss/15118398/research-and-residency-position-in-therapeutic-medical-physics New York, New York, An opening is now available postdoctoral position working on a project entitled, Marker-less Tumor Tracking for Paraspinal and Lung SBRT Treatment. The ideal candidate should have strong physics or mathematical background and be proficient in certain programming language such as C/C++, Python, Tensorflow/PyTroch, or MATLAB. Knowledge in medical imaging or image processing is a plus. The research will focus on developing motion tracking algorithms that can be used in radiation therapy. The candidate will work closely with medical physicists and radiation oncologists in developing the methods applied to lung cancer treatment and paraspinal stereotactic body radiation therapy. There will also be great opportunity for the candidate to get the firsthand knowledge & experiences of using deep learning in the field of radiation therapy. This is a full-time two-year appointment. For the right candidate an opportunity to join combined four-year hybrid research/residency program in Therapeutic Medical Physics in the Department of Medical Physics is available. Details of this program are available at https://www.mskcc.org/hcp-education-training/residencies/residency-therapeutic-medical-physics . The Department of Medical Physics consists of over forty faculty physicists and computer scientists plus support staff working on various physical problems related to diagnosis and therapy for cancer. MSKCC has a large, cutting edge program in all aspects of radiation oncology physics that seeks to improve the clinical effectiveness of radiation therapy in partnership with radiation oncologists, radiologists and other medical professionals. Many new programs in radiation therapy research and development are ongoing, including: the development and clinical use of predictive models (tumor control and normal tissue complication probability) in treatment planning, improved treatment planning optimization algorithm, integration of MR and PET imaging into radiotherapy decision making and treatment planning, 4D imaging and motion management, and the development of informatics-based and adaptive radiotherapy processes ( www.mskcc.or/departments/medical-physics ). In 2019, MSK enterprise-wide radiation and medical physics resources will include twenty-nine linear accelerators, one MR-Linac, six HDR units, CT, PET/CT and MRI simulators, and state of the art inter- and intra-fractional imaging and motion management capabilities. We are also partnered with the New York Proton Center, that houses one cyclotron, three rotational gantry treatment rooms, one fixed beam treatment room, one future research beam room, related PTEV support service spaces, PET/CT, two CTs, two MRIs, related clinical support space. We have a strong philosophy that all facilities will provide outstanding treatment quality as well as contribute to the overall mission of MSKCC to advance the state of cancer care. Details of the residency program can be found at https://www.mskcc.org/hcp-education-training/residencies/residency-therapeutic-medical-physics . The successful candidate will be compensated according to the MSKCC standard rates based upon experience. Specifics information on employee benefits offered may be found at https://careers.mskcc.org/learn-about-msk/benefits/ . Interested candidates should include CV, letter of interest and list of three references with thier application.Please address any additional questions to Christopher J. Watchman, PhD, DABR, Education Director and Associate Attending Physicist, watchmac@mskcc.org. #LI-POST Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15118370/senior-research-technician https://jobboard.globalhealth.org/jobs/rss/15118370/senior-research-technician New York, New York, Are you looking for a new and exciting opportunity? We might have the ideal one for you! As a Senior Research Technician you will perform research activities in collaboration with internal/external personnel to complete science-based projects. You will normally receive detailed instructions while making observations, analyzing data and interpreting results according to laboratory procedures. We will give you the tools to provide support to all technical/research staff and postdocs. You are: Effective at communicating, capable of resolving how best to reach different audiences and executing communications based on that understanding Adept at planning and prioritizing work to meet commitments with a keen eye for detail Eager to seek new opportunities and tough challenges with high energy, and passion You will: Prepare laboratory equipment and work with cultures and/or cell separation methods; electrophoretic separations: assays (e.g., RIA, TIA, ELISA); basic biology or other niche science techniques depending on the lab. Operate lab equipment such as centrifuges, pH meters, analytical balancers, scintillation counters, spectrophotometers, light microscopes and other equipment as taught. Assist in animal handling requiring injection of animals, collection/harvesting of tissues, fluids; animal autopsies in order to make chemical identification and conduct analyses. Complete tasks with the mentorship of your P.I. and staff associated with designated research projects by carrying out the requested activities. Provide assistance with other ongoing research for peers and research personnel in the laboratory by completing tasks related to the projects. Perform vital analysis and calculations, record data and write reports on research findings. Respond to and produce reports comprising of the requested statistics for the study as requested by the laboratory head and members of the research team. You have! We are looking for candidates with a Bachelor's in Biology or 3 years of closely related experience #LI-POST Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15066056/clinical-research-supervisor-westchester-and-bergen https://jobboard.globalhealth.org/jobs/rss/15066056/clinical-research-supervisor-westchester-and-bergen West Harrison, New York, We are: The regional research program is responsible for research patient care for study participants enrolled in one or more of over 300+ protocols open in the regional outpatient MSK clinic locations. The long Island Clinical Research supervisor will supervise 12 Clinical Research Specialists at our Bergen and Westchester Regional Care Network and ensure research patient care is facilitated on study while ensuring compliance with all relevant regulatory guidelines from IRB, state and federal law, and Institutional SOPs. The Regional Research Program allows for expanded access to care in communities in the greater NYC area allowing MSK to remain a leader in providing top of the line research patient care. We have an exciting opportunity to join our Regional Research Program for a Clinical Research Supervisor (CRS). You will: Staff Management and Development - Participate in the orientation, training and supervision of CRSps; participate in facilitating departmental trainings; align staff and resources with appropriate protocols and research needs; and maintain workflow consistency among staff with standardized processes. Operation Management - Ensure that workflow is managed and supervised to meet departmental and service needs; Quality Assurance - Perform regular audits to ensure that the data collected is complete and accurate, and that the research projects are carried out as planned. Regulatory Compliance - Ensure that all appropriate Institutional, State, and Federal regulations are followed throughout the course of a research project, database, or protocol. Ensure that research protocols are approved by the Institutional Review Board/Privacy Board (IRB/PB) and followed as written. Data collection - Utilize appropriate methodologies to collect patient/human subject information for research projects, databases, and/or protocols. Data reporting - Generate reports to all vital parties. Prepare data for analysis, supervising visits and audits. Clinical Research Billing Management - Implement Principal Investigator's decisions regarding Patient-Care Costs. Special Projects - Participate or coordinate on both interdepartmental and intra-departmental organization-wide research projects as requested. You will provide leadership, organizational, creative, or clerical support to established and new research initiatives. You Are: Bachelor's degree with at least 3 years of clinical research experience OR a high school diploma with 6 years of clinical research experience Supervisory experience and experience with high volume trials is strongly preferred. Familiar and comfortable with human research protection protocols and guidelines Extensive knowledge and understanding of the regulations pertaining to human subject protection (including 21 CFR and 45 CFR 46 of the United States Code of Federal Regulations) and Health Insurance Portability and Accountability Act (HIPAA) is critical. Strong time management/project management skills. Knowledge of oncology-specific terminology is helpful. Experience in the use of various electronic data management systems. Strong Data management skills, including database design preferred. Basic knowledge of Microsoft suite (PowerPoint, Word, Access, Excel) and Teamshare #LI-POST Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15057300/clinical-research-project-associate-pcctc-100-remote https://jobboard.globalhealth.org/jobs/rss/15057300/clinical-research-project-associate-pcctc-100-remote New York, New York, The Prostate Cancer Clinical Trials Consortium (PCCTC) is hiring a Clinical Research Project Associate. In this role, you will be responsible for providing support to the Clinical Operations team for multi-center clinical trial activities from concept to close-out. You will: Manage complex multi-institutional clinical trials across a diverse research portfolio. Assist in overseeing clinical trials including protocol and informed consent drafting, regulatory document drafting, etc. Communicate effectively and establish strong working relationships with a diverse matrix of clinical trial sites, investigators, pharmaceutical & biotechnology partners, and other important stakeholders. Sustain project workflows and timelines, ensuring deadlines and milestones are met. Maintain comprehensive, GCP/FDA compliant, Trial Master Files for assigned projects. Manage regulatory approvals (ex. IRB), review and filing of documents for Trial Master Files for projects. Synthesize complex clinical, regulatory, and other clinical trial information into actionable plans. Provide necessary documentation in compliance with existing standard operating procedures, regulatory guidelines, etc. Assist in maintaining necessary clinical trial conduct documentation (includes Project Management Plans, Safety Management Plans, Monitoring Plans, Meeting Minutes, etc.). Communicate and work effectively with all stakeholders of the PCCTC - Clinical Operations, Data Management, Business Management, Budgets & Contracts, Editorial, etc. You Are: Adept at planning and prioritizing work to meet commitments aligned with organizational goals. An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding. Comfortable working in a fast-paced environment. Adept at building partnerships and working collaboratively with others to meet shared objectives and goals. You Have: A Bachelor's degree (preferred) with least 2-4 year of clinical research experience. Proven ability to manage clinical research projects with strict deadlines. Working knowledge of the Code of Federal Regulations, Good Clinical Practice, and Human Subjects Protection. Knowledge of clinical trial regulatory and safety management preferred. Strong computing skills including proficiency in MS Office products. Ability to solve problems by using a logical, systematic, sequential approach. Ability to work productively in a remote work environment. Experience working with prostate cancer clinical trials and/or multicenter projects is a plus. Benefits Competitive compensation packages | Sick Time |Generous Vacation+ 12 holidays to recharge & refuel| Internal Career Mobility & Performance Consulting | Medical, Dental, Vision, FSA & Dependent Care|403b Retirement Savings Plan Match|Tuition Reimbursement |Parental Leave & Adoption Assistance |Commuter Spending Account |Fitness Discounts &Wellness Program | Resource Networks| Life Insurance & Disability | Remote Flexibility We believe in communication, openness, and thinking beyond your 8-hour day @ MSK. Its important to us that you have a sense of impact, community, and work/life balance to be and feel your best. Our Hiring Process You review the posting, agree it sounds like a great fit & apply ->Talent Acquisition contacts you to schedule a phone interview (if your profile aligns) -> after speaking with the Talent Acquisition Specialist, you will connect with the Hiring Manager by phone or video -> if your experience is a fit, you will move forward to a video call or on-site visit with the team -> post-interview feedback->ideally an offer! ->reference check & onboarding-> orientation & official welcome to MSK. #LI-POST Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15096057/community-outreach-assistant-immigrant-health-cancer-disparities-service https://jobboard.globalhealth.org/jobs/rss/15096057/community-outreach-assistant-immigrant-health-cancer-disparities-service New York, New York, The Department of Psychiatry and Behavioral Sciences serves and supports the mission of Memorial Sloan Kettering, which is: To lead in the prevention, diagnosis, treatment, and cure of cancer through programs of excellence in research, education, outreach, and cost-effective patient care. The Immigrant Health and Cancer Disparities (IHCD) Service within the department works to address disparities in access to cancer treatment and other healthcare services at the local, national, and global levels. We use a cross-disciplinary, community-engaged approach. We identify key areas of need and provide health education and other services to immigrants and medically underserved communities. We are seeking a Community Outreach Assistant (COA), to join our team. The COA plays a vital role within the Immigrant Health and Cancer Disparities Service, Department of Psychiatry, and Behavioral Sciences. The assistant executes outreach research programs and protocols. As an integral member of the research team and in compliance with all regulatory, institutional, and departmental requirements, performs data collection, data entry, and data analysis for research projects, databases, and research protocols for the IHCD Service. Maintains close relationships with agencies and institutional staff. Conducts research programs/protocols within appropriate guidelines and regulations. Ensure data quality and integrity during each phase of data collection and for each protocol assigned. You Will: Participate in outreach with French speaking immigrant-serving health care facilities, community-based organizations, advocacy groups, ethnic media, and local government leaders Assist with the creation of monthly reports of outreach, research, and educational activities Attend training programs, modules, workshops, seminars, disease-specific meetings, and meetings to keep up-to-date on project objectives and new policies/procedures for conducting Community Outreach / human subjects research, when directed by supervisor Ensure that the consent/research authorization documents are signed and maintained as per protocol/department/service/MSK/agency policies. Work with community organizations and their members to expand outreach Maintain collaborative relationships with community groups and community leaders by supporting local initiatives and events Participate in community events for Spanish-speaking communities and other immigrant communities Work on special research initiatives including special requests for Research Council, IRB, Office of Clinical Research, or any regulatory compliance projects You Are: An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding Adept at creating partnerships and working collaboratively to meet shared objectives and goals Capable of building strong customer relationships and delivering customer-centric solutions A good decision-maker, with shown success at making timely decisions that keep the organization moving forward Willing to take action and eager to accept new opportunities and tough challenges with high energy, and passion You Have: Fluency in French Minimum of a high school diploma plus 2 years of experience working in or with community-based outreach research with a focus on service and research health-related programs strongly preferred Proven interest in health disparities; knowledge of immigrant communities Strong program management and organizational skills Knowledge of SPSS a plus Monday-Friday; 9:00am-5:00pm with flexibility #LI-Post Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15074996/clinical-research-associate-gmo-women-s-health-service https://jobboard.globalhealth.org/jobs/rss/15074996/clinical-research-associate-gmo-women-s-health-service New York, New York, Do you have at least 1 years of working in Clinical Trials? Are you seeking an opportunity to be at the forefront of innovation during this exciting time at Memorial Sloan Kettering Cancer Center? This is a great role for someone who has the right skills, who wants to be part of a dynamic team and who wants to learn how to apply their skills to support our mission: the progressive control and cure of cancer through programs of patient care, research, and education. https://youtu.be/9R7QoNfmm0w We have an exciting opportunity in our Women's Health-GMO Service as a Clinical Research Associate. As an integral member of the research team, and in compliance with all regulatory, institutional, and departmental requirements, the Clinical Research Associate (CRA ) coordinates and maintains the assigned research portfolio for a Service and/or Department. You Will: Serve as the main point of contact for all research portfolio activities, and maintain real-time knowledge of every aspect of all research protocols. Be the critical facilitator for a multidisciplinary team encompassing data and patient management, as well as regulatory oversight. Effectively communicate the overall study progress to various internal and/or external stakeholders, and identify study trends and create/implement solutions. Perform diverse research-related functions using sound judgment and exceptional organizational skills. You are: Adept at anticipating and prioritizing work to meet commitments of multiple stakeholders. Adept at building partnerships and working collaboratively to influence others to meet shared objectives and goals. Known as someone who improves processes and proactively, independently identifies solutions that anticipate stakeholder needs. You have: HS Diploma/GED with 2-4 years relevant work experience as part of a clinical trial research team, managing protocols, and/or handling data audits and regulatory, OR Bachelors Degree with at least 1 full year of relevant work experience as part of a clinical trial research team, managing protocols, and/or handling data audits and regulatory. Good Clinical Practice (GCP) and Human Subjects Protection (HSP) Certifications required. Proficiency with the Electronic Medical Record (EMR) system. Excellent computer skills, including proficiency in Microsoft Office Products and other software programs for database management/queries, generating reports and developing graphics. Knowledge of clinical research data collection processes in accordance with GCP. Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15062645/clinical-research-associate-dermatology https://jobboard.globalhealth.org/jobs/rss/15062645/clinical-research-associate-dermatology New York, New York, Are you seeking an opportunity to be at the forefront of innovation during this exciting time at Memorial Sloan Kettering Cancer Center? This is a great role for someone who has the right skills, who wants to be part of a dynamic team and who wants to learn how to apply their skills to support our mission: the progressive control and cure of cancer through programs of patient care, research, and education. https://youtu.be/9R7QoNfmm0w We have an exciting opportunity in our Dermatology Service within the Department of Medicine as a Clinical Research Associate. As an integral member of the research team, and in compliance with all regulatory, institutional, and departmental requirements, the Clinical Research Associate (CRA ) coordinates and maintains the assigned research portfolio for a Service and/or Department. You Will: Serve as the main point of contact for all research portfolio activities, and maintain real-time knowledge of every aspect of all research protocols. Be the critical facilitator for a multidisciplinary team encompassing data and patient management, as well as regulatory oversight. Effectively communicate the overall study progress to various internal and/or external stakeholders, and identify study trends and create/implement solutions. Perform diverse research-related functions using sound judgment and exceptional organizational skills. You are: Adept at anticipating and prioritizing work to meet commitments of multiple stakeholders. Adept at building partnerships and working collaboratively to influence others to meet shared objectives and goals. Known as someone who improves processes and proactively, independently identifies solutions that anticipate stakeholder needs. You have: HS Diploma/GED with 2-4 years relevant work experience as part of a clinical trial research team, managing protocols, and/or handling data audits and regulatory, OR Bachelors Degree with at least 1 full year of relevant work experience as part of a clinical trial research team, managing protocols, and/or handling data audits and regulatory. Good Clinical Practice (GCP) and Human Subjects Protection (HSP) Certifications required. Proficiency with the Electronic Medical Record (EMR) system. Excellent computer skills, including proficiency in Microsoft Office Products and other software programs for database management/queries, generating reports and developing graphics. Knowledge of clinical research data collection processes in accordance with GCP. Wed, 14 Jul 2021 03:01:48 -0400 https://jobboard.globalhealth.org/jobs/rss/15042943/clinical-research-associate-myeloma https://jobboard.globalhealth.org/jobs/rss/15042943/clinical-research-associate-myeloma New York, New York, Are you seeking an opportunity to be at the forefront of innovation during this exciting time at Memorial Sloan Kettering Cancer Center? This is a great role for someone who has the right skills, who wants to be part of a dynamic team and who wants to learn how to apply their skills to support our mission: the progressive control and cure of cancer through programs of patient care, research, and education. https://youtu.be/9R7QoNfmm0w We have an exciting opportunity in our Myeloma Service Department of Medicine as a Clinical Research Associate. As an integral member of the research team, and in compliance with all regulatory, institutional, and departmental requirements, the Clinical Research Associate (CRA ) coordinates and maintains the assigned research portfolio for a Service and/or Department. You Will: Serve as the main point of contact for all research portfolio activities, and maintain real-time knowledge of every aspect of all research protocols. Be the critical facilitator for a multidisciplinary team encompassing data and patient management, as well as regulatory oversight. Effectively communicate the overall study progress to various internal and/or external stakeholders, and identify study trends and create/implement solutions. Perform diverse research-related functions using sound judgment and exceptional organizational skills. You are: Adept at anticipating and prioritizing work to meet commitments of multiple stakeholders. Adept at building partnerships and working collaboratively to influence others to meet shared objectives and goals. Known as someone who improves processes and proactively, independently identifies solutions that anticipate stakeholder needs. You have: HS Diploma/GED with 2-4 years relevant work experience as part of a clinical trial research team, managing protocols, and/or handling data audits and regulatory, OR Bachelors Degree with at least 1 full year of relevant work experience as part of a clinical trial research team, managing protocols, and/or handling data audits and regulatory. Good Clinical Practice (GCP) and Human Subjects Protection (HSP) Certifications required. Proficiency with the Electronic Medical Record (EMR) system. Excellent computer skills, including proficiency in Microsoft Office Products and other software programs for database management/queries, generating reports and developing graphics. Knowledge of clinical research data collection processes in accordance with GCP. Wed, 14 Jul 2021 03:01:48 -0400