Senior Clinical Research Coordinator

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This range is provided by Massachusetts General Hospital. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

$49,504.00/yr - $72,404.80/yr

Massachusetts General Hospital and Harvard Medical School are seeking a highly motivated candidate to join the Immunobiology Laboratory. The role focuses on innovative clinical trials for the treatment of type 1 diabetes using the BCG vaccine, with opportunities to gain hands‑on experience in regulatory medicine and translational research. Full time, 100% onsite and predominately early morning visits starting at 7:00 AM, M‑F.

Anticipated working hours are 7 AM‑4 PM.

The CRC‑Senior will oversee program‑wide regulatory and operational needs across multiple supportive care research studies. In addition to contributing to projects employing qualitative methods, survey data, and clinical trial designs, the CRC‑Senior will help develop and implement standard operating procedures, onboard and train junior clinical research coordinators (CRCs), and ensure high‑quality study execution and compliance. This position is ideal for candidates with prior research experience who are ready to take on supervisory and program development responsibilities.

• Train, and mentor entry‑level CRCs, ensuring adherence to standard operating procedures and best practices.

• Provide an extra layer of support in managing studies, including participant eligibility reviews, recruitment, informed consent, and coordination of study visits.
• Assist with data collection (surveys, interviews, chart reviews) and quality control checks, using REDCap (Research Electronic Data Capture) or other programs.

• Prepare and maintain Institutional Review Board (IRB) protocol submissions, amendments, continuing reviews, and adverse event reports.
• Ensure compliance with study protocols, Human Subjects and Good Clinical Practice guidelines, and institutional policies.
• Assist in coordinating Data Safety Monitoring Board (DSMB) meetings.
• Update and review Standard Operating Procedures (SOPs).

• Assist in developing standard operating procedures and quality assurance systems.
• Contribute to creation of study templates and guidance for protocol design, database management, and grant submissions.

• Bachelor’s degree required (health sciences, psychology, public health, nursing, or related field preferred)
• Minimum of 5 years of post‑baccalaureate research experience in clinical trials or human subjects research, including direct experience with IRB/regulatory documentation.
• Ability to oversee, train and evaluate others effectively.
• Strong organizational, time management, and problem‑solving skills.
• Excellent interpersonal and written/verbal communication skills.
• Ability to work independently and collaboratively across multiple investigators and teams.
• Familiarity with REDCap and other data capture systems preferred.

• Mid‑Senior level

• Full‑time

• Research, Analyst, and Information Technology

• Hospitals and Health Care