Clinical Research Coordinator responsible for clinical trial oversight at Thomas Jefferson University. Ensuring compliance with regulations and managing daily clinical research operations.
Responsibilities
Responsible for the coordination and oversight of clinical research trials from start-up through close-out.
Ensure compliance with Institutional Review Boards (IRB), FDA, and other regulations governing human subject research.
Prepare and submit regulatory documents, amendments, and safety reports.
Lead daily clinical research operations and ensure activities follow approved study protocols.
Oversee participant recruitment, screening, informed consent, and enrollment.
Requirements
High School Diploma or equivalent and SoCRA certification and 6 years of clinical research experience or Bachelor’s degree and 2 years of clinical research experience or Master’s Degree and 1 year clinical research experience
Benefits
medical (including prescription) insurance
supplemental insurance
dental
vision
life and AD&D insurance
short- and long-term disability
flexible spending accounts
retirement plans
tuition assistance
medical (including prescription) insurance access for part-time colleagues
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