- San Antonio, Texas, United States
- On-site
- Full-time · Mid
The Clinical Research Coordinator (CRC) - Intermediate champions patient safety and protocol integrity while upholding the highest standards of patient care, coordinating all on-study activities for clinical trials.
Responsibilities
- Screening and scheduling patients
- Coordinating all on-study activities
- Maintaining compliance with study requirements
- Participating in study teleconferences with sponsors and clinical research organizations
- Ensuring timely and accurate reporting of serious adverse events, unanticipated problems, deviations, and noncompliance to the IRB and study sponsor
Requirements
- Bachelor's degree
- Nice to have: Knowledge of Federal regulations and ethical standards governing human subjects research (e.g., FDA, HIPAA, IRB processes)
- Nice to have: Basic understanding of Clinical trial design, methodology, and protocol requirements