- Baltimore, Maryland, United States
- On-site
- 3+ years
Clinical Research Coordinator (CRC) responsible for day‑to‑day coordination and execution of assigned clinical trials.
Responsibilities
- Coordinate and execute assigned clinical research studies from feasibility and study start‑up through study conduct and close‑out
- Serve as a primary site contact for sponsors, CROs, IRBs/IECs, and study vendors
- Manage day‑to‑day clinical trial operations and maintain communication with the Principal Investigator
- Recruit and pre‑screen potential participants and support informed consent process
- Coordinate participant study visits, retention, and follow‑up activities
Requirements
- Bachelor’s degree in life sciences, nursing, healthcare, or a related field
- Nice to have: Certified Clinical Research Coordinator (CCRC)
- Nice to have: Certified Clinical Research Professional (CCRP)
- Nice to have: Phase I–IV industry‑sponsored clinical trials
- Nice to have: Allergy/Immunology experience