Clinical Research Coordinator - Data & Compliance Lead

UMass Med School; Worcester (MA); In loco; USD 65.000 - 90.000; Tempo pieno

Descrizione del lavoro

UMass Med School is seeking a Clinical Research Coordinator III to independently perform delegated tasks in human subject research under the PI. The role involves coordinating regulatory activities and data management for complex protocols across treatment, ancillary services, and prevention practices.

Responsibilities include consent, subject recruitment, scheduling visits, maintaining regulatory documentation, training staff, and contributing to grant preparation and IRB processes.

Competenze

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

Mansioni

• Obtain consent of research participants in accordance with IRB protocols and HIPAA.
• Assist with recruiting, screening, selecting, maintaining and terminating study subjects for multiple protocols.
• Identify, schedule and conduct participant study visits, tests and interviews/phone follow ups.

Conoscenze

3-5 years of related experience

Travel ability

Formazione

Bachelor's degree in a scientific or health related field

Descrizione del lavoro

UMass Med School is seeking a Clinical Research Coordinator III to independently perform delegated tasks in human subject research under the PI. The role involves coordinating regulatory activities and data management for complex protocols across treatment, ancillary services, and prevention practices.

Responsibilities include consent, subject recruitment, scheduling visits, maintaining regulatory documentation, training staff, and contributing to grant preparation and IRB processes.