As a Research Project Associate in Multicenter Office Compliance, you will provide data analysis and project assistance for research protocols. You will be responsible for data/project management activities and for data accuracy and integrity associated with clinical research. You will also participate in special projects as determined by management.
Manages internal and external inquiries regarding MSK sponsored Multicenter studies and directs to area expert when needed.
Generate reports to all necessary parties on the progress of the research project, database, or protocol, as needed.
Assist in managing departmental data.
Perform regular reviews to ensure that the data collected is complete and accurate and to ensure that the research project was carried out as outlined.
Communicates with staff at all levels (principal investigators, clinical and research support staff).
Assist in protocol audits- reviewing and collecting regulatory documents, provide data entry assistance if needed.
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.
Provide leadership, organizational, creative, or clerical support to established and new research initiatives.
Participate in special projects and task forces as determined by management.
Participates in talent management: interviewing, hiring, orienting, training, and supervision of one direct report.
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
Adept at learning quickly, applying insights from past efforts to new situations.
An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understanding.
Action-oriented and eager to embrace new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm.
A High School Diploma/GED, or Bachelor's preferred
A minimum of a High School Diploma with at least 3 - 4 years MSKCC clinical research experience.
Experience in clinical research and/or other applicable research investigation. Relevant graduate work would be considered in lieu of minimum experience.
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).
At Memorial Sloan Kettering (MSK), we’re not only changing the way we treat cancer, but also the way the world thinks about it. By working together and pushing forward with innovation and discovery, we’re driving excellence and improving outcomes. For the 28th year, MSK has been named a top hospital for cancer by U.S. News & World Report. We are proud to be on Becker’s Healthcare list as one of the 150 Great Places to Work in Healthcare in 2018, as well as one of Glassdoor’s Employees’ Choice Best Place to Work for 2018. We’re treating cancer, one patient at a time. Join us and make a difference every day.