Clinical Research Coordinator I: Study Operations & Compliance

University of Massachusetts Medical School; Worcester (MA); On-site; USD 40,000 - 55,000; Full time

Benefits offered by this job

Paid time off

Medical, dental, and vision coverage

401(a) retirement plan

Voluntary 403(b) plan

Job summary

The University of Massachusetts Medical School is seeking a candidate for a research role that involves obtaining consent from study participants and ensuring compliance with regulatory protocols. The role demands a Bachelor's degree in a scientific or health-related field, alongside the ability to travel to off-site locations. Responsibilities include tracking study enrollment, maintaining regulatory documentation, and assisting with various operational aspects of research. A comprehensive benefits package is offered, including paid time off and medical coverage.

Qualifications

• Bachelor’s degree in a scientific or health-related field, or equivalent experience.
• 0–1 year of related experience.
• Ability to travel to off-site locations.

Responsibilities

• Obtain consent of research participants in accordance with the IRB-approved protocols.
• Identify, schedule and/or conduct participant study visits, interviews, and tests.
• Maintain all regulatory documentation, including local or central IRB and study data.

Education

Bachelor’s degree in a scientific or health-related field

0–1 year of related experience

Job description

The University of Massachusetts Medical School is seeking a candidate for a research role that involves obtaining consent from study participants and ensuring compliance with regulatory protocols. The role demands a Bachelor's degree in a scientific or health-related field, alongside the ability to travel to off-site locations. Responsibilities include tracking study enrollment, maintaining regulatory documentation, and assisting with various operational aspects of research. A comprehensive benefits package is offered, including paid time off and medical coverage.