Sr. Clinical Research Coordinator

Job Summary

The Center for Precision Psychiatry (CPP) at Mass General Hospital is seeking applications for a full-time Sr. Clinical Research Coordinator (CRC) to coordinate and administer projects led by Dr. Susan Whitfield-Gabrieli. This position is particularly well-suited for anyone interested in pursuing graduate study in the fields of psychology, public health, neuroscience, or medicine.

Qualifications

• Education: Bachelor's Degree in a related field
• Experience: Prior experience within the Research Protocols 2-3 years preferred and Previous Research Experience 3-5 years required
• Licenses and Credentials: Experience in lieu of a degree may be accepted

Essential Functions

• Works very independently under minimal supervision to enroll eligible patients in 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.
• Afford assistance in the areas of Quality Control, Training, & Development and may provide input into the assessment of departmental procedures.
• The position involves a combination of data abstraction and entry, regulatory management, and patient coordination.
• Aid the clinical team in screening potential patients for study participation.
• Maintain point of contact communication with enrolled patients and assist with front-line questions regarding study participation.
• 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.
• Obtain protocol clarifications from the study sponsor and communicate information to the research team.
• Organize and prepare for internal and external audits.
• Prepare and submit protocol amendments, continuing reviews, and safety reports to the IRB.
• Revise informed consent documents to include new risk information and/or updated protocol requirements through the course of the study.

Additional Job Details

(if Applicable)

Pay Range

$50,502.40 - $82,014.40/Annual

Grade

6