Clinical Research Coordinator I - Regulatory & Data Support

University of Massachusetts Medical School; Worcester (MA); On-site; USD 50,000 - 70,000; Full time

Benefits offered by this job

Paid time off

Medical coverage

Dental coverage

Vision coverage

Participation in retirement plan

Job summary

A leading medical university in Worcester, Massachusetts is seeking a Clinical Research Coordinator I to manage regulatory activities and data for human subject research. Responsibilities include obtaining participant consent, maintaining documentation, and assisting with grant operations. Candidates should have a Bachelor's degree in a scientific or health-related field and 0-1 year of relevant experience. The position offers a comprehensive benefits package including medical, dental, and retirement plan participation.

Qualifications

• Bachelor's degree in a scientific or health-related field, or equivalent experience.
• 0-1 year of related experience.

Responsibilities

• Obtain consent of research participants in accordance with IRB-approved protocols.
• Identify and conduct participant study visits, interviews, and tests.
• Maintain all regulatory documentation, including IRB and study data.
• Assist with financial/operational aspects of grants and contracts.
• Track and maintain study-related information in the data management system.

Skills

Ability to travel to off-site locations

Education

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

Job description

A leading medical university in Worcester, Massachusetts is seeking a Clinical Research Coordinator I to manage regulatory activities and data for human subject research. Responsibilities include obtaining participant consent, maintaining documentation, and assisting with grant operations. Candidates should have a Bachelor's degree in a scientific or health-related field and 0-1 year of relevant experience. The position offers a comprehensive benefits package including medical, dental, and retirement plan participation.