Drimva

Jefferson Health

Clinical Research Coordinator (OB-GYNE)

Philadelphia, PA · Full-time · Posted Mar 11, 2026

Experience
4 years of relevant experience with a high school diploma or equivalent; alternatively, a bachelor’s or master’s degree and previous experience preferred.
Education
High school diploma or equivalent; alternatively, a bachelor’s or master’s degree.

About the job

Supports day-to-day clinical trial operations by coordinating study visits and consent, managing research data and biospecimens, and assisting investigators with documentation and regulatory filings.

What you'll do

  • Conducts recruitment, consent assistance, and study visits; may assist with human-subject enrollment.
  • Performs research activities including database management, biospecimen collection and processing, and clerical support; maintains trial documentation.
  • Reports patient responses and adverse effects to the Principal Investigator and assists with IRB and other regulatory filings.

What they ask for

  • High school diploma or equivalent and 4 years of relevant experience, or a bachelor’s/master’s degree with previous experience preferred.
  • Works in accordance with Good Clinical Research Practice (GCP) and clinical trial protocols.

Nice to have

  • Bachelor’s or master’s degree.
  • Previous experience.

Tools

Good Clinical Research Practice (GCP)

Model-written summary · the original posting is authoritative

First seen Oct 14, 2026 · Last verified Nov 6, 2026 (UTC)