Clinical Research Coordinator: Drive Study Data & Compliance

University of Massachusetts Medical School; Worcester (MA); Hybrid; USD 55,000 - 85,000; Full time

Benefits offered by this job

Total Rewards package

Paid time off

Medical, dental, and vision coverage

Job summary

UMass Chan Medical School is seeking a Clinical Research Coordinator at multiple levels to work under the PI on human subject research and data management. The role involves coordinating regulatory activities, data collection, and ensuring protocol compliance across studies related to treatment, prevention, and services.

The position offers growth from CRC I to Sr CRC, with responsibilities including consent, scheduling visits, regulatory documentation, and collaboration with investigators and

Qualifications

• Bachelor's degree in a scientific or health-related field or equivalent experience.
• 0-1 year of related experience (CRC I).
• 1-3 years of related experience (CRC II).
• 3-5 years of related experience (CRC III).
• 5-7 years of related experience (Sr Clinical Research Coord).
• Ability to travel off-site locations.

Responsibilities

• Obtain consent of research participants per IRB protocols.
• Identify and schedule participant visits and follow-ups.
• Maintain regulatory documentation and data for study.
• Track enrollment and study milestones.
• Assist with grant preparation and IRB processes.
• Ensure adherence to GCP and confidentiality standards.

Skills

Regulatory coordination

IRB/data management

Study coordination

Communication

Education

Bachelor's degree in scientific or health-related field

Job description

UMass Chan Medical School is seeking a Clinical Research Coordinator at multiple levels to work under the PI on human subject research and data management. The role involves coordinating regulatory activities, data collection, and ensuring protocol compliance across studies related to treatment, prevention, and services.

The position offers growth from CRC I to Sr CRC, with responsibilities including consent, scheduling visits, regulatory documentation, and collaboration with investigators and