Jefferson Health
Clinical Research Coordinator Sr. (Remote)
Philadelphia, PA · Senior · Full-time · Posted Oct 13, 2026
- Experience
- 6 years with a High School Diploma/GED and SoCRA, or 2 years with a Bachelor’s degree, or 1 year with a Master’s Degree.
- Education
- High School Diploma/GED; stated alternatives include a Bachelor’s degree or Master’s Degree.
About the job
Provides regulatory support for oncology clinical trials, including preparing and submitting study documents and maintaining complete, current regulatory files.
What you'll do
- Acts as the regulatory contact for assigned protocols and communicates with IRBs, sponsors, and study teams.
- Prepares and submits protocols, amendments, and continuing review applications to PRMC and IRBs; coordinates submissions to ancillary committees.
- Maintains regulatory files and version control, and prepares files for audits and monitoring visits.
What they ask for
- High School Diploma/GED.
- Clinical research experience under one of the stated pathways: 6 years with a High School Diploma/GED and SoCRA; 2 years with a Bachelor’s degree; or 1 year with a Master’s Degree.
Tools
PRMC, IRB
Model-written summary · the original posting is authoritative