Upvote
Downvote
Clinical Research Coordinator
Share Job
- Suggest Revision
Full-time
- We care for one another, find new ideas to accelerate medicine, and seed a long-term impact for generations.
- The Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
- Ensure adequate supplies have arrived on site for protocol initiation (lab kits, study medication, specialized equipment, IVRS/EDC access and passwords)
- Identify adverse events (AEs) and Serious Adverse Events (SAEs) and promptly notify Principal Investigator and Sponsor (where appropriate)
- Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel.
Active Job
Updated 1 month agoSimilar Job
Relevance
Active