What are the responsibilities and job description for the Clinical Research Coordinator - On-Site position at Seacrest Behavioral Health?
This on-site clinical research coordinator role in Bountiful, Utah involves managing multiple trials of varying complexity, performing clinical procedures, and overseeing study activities.
Key Responsibilities Include
Key Responsibilities Include
- Managing 2-6 concurrent trials across different therapeutic areas
- Patient recruitment, obtaining informed consent, and handling regulatory documentation
- Performing clinical procedures such as vital signs, phlebotomy, and ECGs
- Coordinating study activities from initiation to completion and during site audits
- Mentoring junior staff and supporting internal training initiatives
- 1-3 years of clinical research experience at an investigative site (CRC I level) or more for CRC II
- Proficiency in vital signs, phlebotomy, ECGs, and specimen processing
- Excellent written and verbal communication with strong attention to detail
- Understanding of site operations and drug development processes
- Competency with CTMS, eCRF systems, and Microsoft Office
Salary : $36,600 - $91,300