Clinical Research Coordinator III — Study Oversight & Data Quality

UMass Chan Medical School; Shrewsbury (MA); On-site; USD 65,000 - 90,000; Full time

Job summary

UMass Chan Medical School is seeking a Clinical Research Coordinator III to independently manage delegated tasks for complex human subjects research. You will coordinate regulatory activities, collect and manage data, and support investigators across multiple protocols in treatment, prevention, and ancillary services.

You will obtain participant consent, assist with recruitment, schedule visits, and ensure accuracy of regulatory documentation, while training staff and monitoring compliance with

Qualifications

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

Responsibilities

• Obtain consent of research participants per IRB protocols and HIPAA.
• Assist with recruiting, screening, and maintaining study subjects.
• Schedule and conduct participant visits, tests, and follow-up interviews.
• Ensure regulatory documentation and data support for investigators and sponsors.
• Direct training of staff and oversight of research support personnel.
• Monitor protocol compliance and assist with grant and contract processes.

Skills

Regulatory coordination

Data management

Study recruitment

Education

Bachelor's degree in a scientific or health related field

Job description

UMass Chan Medical School is seeking a Clinical Research Coordinator III to independently manage delegated tasks for complex human subjects research. You will coordinate regulatory activities, collect and manage data, and support investigators across multiple protocols in treatment, prevention, and ancillary services.

You will obtain participant consent, assist with recruitment, schedule visits, and ensure accuracy of regulatory documentation, while training staff and monitoring compliance with