Thomas Jefferson University - Philadelphia, PA
posted 8 days ago
Full-time - Entry Level
Philadelphia, PA
10,001+ employees
Educational Services
About the position
The Clinical Trial Coordinator at Jefferson is responsible for overseeing the daily activities of clinical trials, ensuring compliance with Good Clinical Research Practice (GCP). This role involves a variety of research activities, including database management, biological specimen processing, and clerical duties, to support investigators in organizing and compiling clinical research data. The coordinator will also assist in recruiting subjects, obtaining consent, and conducting study visits.
Responsibilities
- Oversee the day-to-day activities of clinical trials in accordance with Good Clinical Research Practice (GCP).
- Perform research activities including database management and biological specimen processing.
- Organize and maintain documentation required for clinical trials.
- Inform the Principal Investigator about any issues concerning patient responses to treatment or adverse effects.
- Assist the Principal Investigator with regulatory body filings, including IRB submissions.
- Assist in the enrollment of human subjects for clinical trials.
- Provide clerical and technical support to ensure adherence to research protocols.
Requirements
- Minimum High School Diploma or equivalent required.
- 4 years of relevant experience or a Bachelor's/Master's degree with previous experience preferred.
Nice-to-haves
- Experience in clinical research or trials.
- Knowledge of regulatory requirements for clinical trials.
Benefits
- Equal access to employment opportunities.
- Commitment to diversity and inclusion in the workplace.
