Clinical Research Coordinator I or II
About The Position
Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham. Replacement for Isabella Larizza Job Summary Summary Works independently under general supervision to enroll eligible patients to clinical research protocols and manage all aspects of data collection and submission for multiple cancer studies. Will be the liaison between the clinical team, sponsor, and Institutional Review Board (IRB) to ensure appropriate communication and reporting. Does this position require Patient Care? No
Requirements
- Bachelor's Degree Related Field of Study required
- Clinical Research or compliance experience 1-2 years preferred
- Ability to work independently and as a team member.
- Analytical skills and ability to resolve problems.
- Ability to interpret acceptability of data results.
- Careful attention to detail.
- Good organizational and communication skills.
- Working knowledge of clinical research protocols.
Responsibilities
- Coordinate patient appointments with physicians, nurses, and all test areas.
- Develop protocol specific flow charts, intake sheets, and other tools to ensure protocol compliance and proper data acquisition.
- Verify adequate documentation of consent, required screening tests and procedures, and eligibility criteria to ensure patients meet all criteria.
- Enroll patients as required by the study sponsor and internal enrollment monitor team.
- Follow patients for the duration of study participation via electronic medical record review to ensure protocol compliance.
- Complete data entry as required for individual study protocols ensuring compliance with institutional and regulatory requirements.
- Monitor and report adverse events and deviations as required by the sponsor, institution, and federal regulations.
- Revise informed consent documents to include new risk information and/or updated protocol requirements through the course of the study.
- Collect, complete, and submit essential regulatory documents to various regulatory entities.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
5,001-10,000 employees
