Clinical Research Coordinator I: IRB & Study Operations

University of Massachusetts Medical School; Worcester (MA); On-site; USD 50,000 - 65,000; Full time

Benefits offered by this job

Paid time off

Medical coverage

Dental coverage

Vision coverage

401(a) retirement plan

Voluntary 403(b) plan

Job summary

The University of Massachusetts Medical School is seeking a Clinical Research Coordinator I to manage research protocols related to human subjects. Responsibilities include securing participant consent, coordinating study visits, and ensuring compliance with regulatory standards. This position requires a Bachelor's degree in a scientific or health-related field and offers a salary complemented by comprehensive benefits including health coverage and retirement plans. Ideal candidates should have 0-1 year of related experience and be willing to travel off-site as necessary.

Qualifications

• 0-1 year of related experience.
• Ability to obtain consent of research participants in accordance with IRB approved protocols.
• Experience with compliance and regulatory documentation.

Responsibilities

• Manage institutional review board submissions and updates.
• Coordinate participant study visits, interviews, and tests.
• Maintain all regulatory documentation.

Skills

Ability to travel off site locations

Education

Bachelor's degree in a scientific or health related field

Job description

The University of Massachusetts Medical School is seeking a Clinical Research Coordinator I to manage research protocols related to human subjects. Responsibilities include securing participant consent, coordinating study visits, and ensuring compliance with regulatory standards. This position requires a Bachelor's degree in a scientific or health-related field and offers a salary complemented by comprehensive benefits including health coverage and retirement plans. Ideal candidates should have 0-1 year of related experience and be willing to travel off-site as necessary.