Brown University Health
Research Regulatory Assistant
$42K–$69K
Rhode Island Hospital · Full-time · Posted Oct 14, 2026
- Experience
- 6 months–1 year in direct clinical trial administration or relevant administrative experience is preferred but not required; an additional 2–3 years of experience may substitute for the bachelor’s degree.
- Education
- Bachelor’s degree in Applied or Life Sciences or related area, including courses in research methodologies and microcomputer systems, or an additional 2–3 years of experience.
About the job
Supports clinical trials by preparing and maintaining regulatory documents and helping manage compliance tasks from study submission through closure.
What you'll do
- Prepare or collect study regulatory documents, process external safety reports, and maintain trial regulatory files and records.
- Process or file IRB and RDC approvals, update the Clinical Trial Management System, and assist with minor study revisions.
- Coordinate with regulatory staff, sponsors, investigators, and research teams, and participate in study initiation and monitoring visits.
What they ask for
- Bachelor’s degree in Applied or Life Sciences or a related area, including courses in research methodologies and microcomputer systems; an additional 2–3 years of experience may substitute.
- Knowledge of research methodology theory and techniques.
- Organizational, interpersonal, teamwork, and written and oral communication skills.
- Proficiency in Microsoft office and various database applications.
Nice to have
- 6 months–1 year of direct clinical trial administration or relevant administrative experience (preferred but not required).
Pay
$41,537.60-$68,556.80 (base salary)
Tools
Microsoft office, Clinical Trial Management System
Model-written summary · the original posting is authoritative