Senior Clinical Research Coordinator — Trials & Compliance

University of Massachusetts Medical School; Shrewsbury (MA); On-site; USD 65,000 - 90,000; Full time

Job summary

University of Massachusetts Medical School is seeking a Clinical Research Coordinator III to independently manage delegated tasks in human subject research, coordinating regulatory activities and data management for complex treatment and prevention protocols.

You will support investigators, sponsors, and auditors, manage study visits and regulatory documentation, and assist with grant preparation and protocol feasibility.

Qualifications

• Bachelor's degree in a scientific or health-related field or equivalent experience.
• 3–5 years of related experience.
• Ability to travel off-site locations.

Responsibilities

• Obtain consent of participants under IRB protocols and HIPAA requirements.
• Assist with recruiting, screening, and maintaining study subjects for multiple protocols.
• Schedule and conduct participant visits, tests, and follow-up calls.
• Ensure accuracy of regulatory documents and data; support investigators and monitors.
• Direct activities of research support staff and assist with staff training.
• Develop study documentation such as questionnaires and data collection tools.
• Contribute to grant preparation, protocol feasibility, manuscript writing, and IRB processes.
• Monitor regulatory compliance and conduct QA reviews of study data.

Skills

Regulatory coordination

Clinical data management

GCP compliance

IRB procedures

Education

Bachelor's degree in science/health

Job description

University of Massachusetts Medical School is seeking a Clinical Research Coordinator III to independently manage delegated tasks in human subject research, coordinating regulatory activities and data management for complex treatment and prevention protocols.

You will support investigators, sponsors, and auditors, manage study visits and regulatory documentation, and assist with grant preparation and protocol feasibility.