Clinical Research Coordinator: Data, Compliance & Study Ops

UMass Chan Medical School; Worcester (MA); On-site; USD 60,000 - 90,000; Full time

Job summary

University of Massachusetts Chan Medical School seeks a Clinical Research Coordinator (CRC) to support human subject research under PI supervision. The role includes coordinating consent, participant visits, data management, and regulatory compliance across multiple protocols.

The position progresses from CRC I to Sr CRC with increasing responsibility for QA, IRB processes, data collection tools, and study leadership activities within the WASLI initiative partnership.

Qualifications

• Bachelors degree in a scientific or health related field, or equivalent experience.
• Experience with coordinating regulatory activities and data collection for human subject research.
• Ability to travel to off-site locations (as needed).

Responsibilities

• Coordinate consent, visits, tests, and follow-ups.
• Maintain regulatory documentation (IRB, study data).
• Track enrollment and study milestones.
• Assist with grant prep, manuscript writing, and IRB processes.

Education

Bachelors degree in a scientific or health related field

Tools

IRB processes

Data management

Regulatory compliance

Job description

University of Massachusetts Chan Medical School seeks a Clinical Research Coordinator (CRC) to support human subject research under PI supervision. The role includes coordinating consent, participant visits, data management, and regulatory compliance across multiple protocols.

The position progresses from CRC I to Sr CRC with increasing responsibility for QA, IRB processes, data collection tools, and study leadership activities within the WASLI initiative partnership.