Upvote
Downvote
Clinical Research Coordinator, on - Site
Share Job
- Suggest Revision
Full-time
- This individual will play a key role in assisting in the conduct of clinical trial activities, in accordance with all applicable regulations governing the conduct of clinical trials.
- Ability to coordinate as primary CRC on at least 1-3 studies of low to medium complexity, with oversight by a manager or higher-level CRC
- Adheres to an IRB approved protocol
- May be asked to perform special project responsibilities and travel to other CCT locations when needs arise
- Complies with IQVIA, CCT, Clinic, and Sponsor policies, standard operating procedures (SOPs) and guidelines
Active Job
Updated 4 days agoSimilar Job
Relevance
Active