We are growing and looking for the perfect candidate to fill our vacant Study Coordinator position.
We would love to speak to you if you have:
Two years of Study Coordinator/Clinical Research Coordinator experience.
Act as the principal administrative liaison for assigned clinical trials.
Project management experience.
As a Study Coordinator, you are responsible for supporting clinical research conducted by a principal investigator(s) at CNS Network. You will assist in project assignments and ensures that pre-established work scope, study protocol, state and federal regulatory requirements, and CNS Network policies and procedures are observed and followed. In addition, act as the principal administrative liaison for assigned clinical trials, ensuring adherence to guidelines for collecting clinical data and administration of clinical studies.
Essential Responsibilities and Duties:
Develops and maintains a relationship professionally and educationally with sponsors, CROs, monitors, investigators, and CNS Network Staff.
Determines feasibility of CNS Network facility to conduct studies in accordance with protocol requirements.
Guides ancillary personnel involved in the planning, implementing, and evaluating clinical studies—assists in training new personnel.
In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings.
Evaluates and interprets collected clinical data in conjunction with the principal investigator(s) as appropriate; prepare oral presentations or written reports and analyses setting forth progress, trends, and appropriate recommendations or conclusions.
Confers with the principal investigator(s) to develop plans for research projects and discuss the interpretation of results; collaborate on preparing manuscripts for publication.
BS or MS degree in the Life Sciences, Psychology, or of related field is required.
Minimum of 2 years of Study Coordinator/Clinical Research Coordinator experience required.
Demonstrated ability to work on deadlines, set priorities, and juggle multiple projects without compromising quality.
Strong project management, analytical, and organizational, and problem-solving skill.
Understanding of ICH and GCP regulations.
Strong interpersonal, people management, and communication skills.
Strong technical expertise with Microsoft Office products (particularly Word, Outlook, and PowerPoint) and Windows XP are essential.
We offer a competitive pay package which includes but not limited to:
401(k)/Dependent Care FSA/EAP
Ancillary Benefits/Group Life Insurance/ AD&D
Employee Engagement Activities/Employee of the Month
As of August 5th, 2021, California State Public Health Officer Order required workers in healthcare settings to be fully vaccinated, with exemptions to religious beliefs or qualified medical reasons, by September 30th, 2021.
Personal protective equipment provided or required.
Social distancing guidelines in place.
Sanitizing, disinfecting, or cleaning procedures in place.
A negative COVID-19 test result is required weekly for individuals who meet the exemption qualification.
If you are interested in working alongside a successful and dynamic team and you meet the following qualifications, we are interested in you! CNS Trials is an equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law.
CNS is a major clinical research center in California. Since first opening its doors in 2000, CNS has been dedicated to searching for a cure, together. By partnering up with major pharmaceutical companies, CNS has been a leader in helping discover tomorrow’s cures for today’s diseases.