Clinical Research Coordinator
IQVIA · Covington, LA +1 more
Clinical OperationsFull-time$38k–$95kCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Clinical Research Coordinator position at an SMO managing multiple clinical trials with exposure to diverse therapeutic areas. Role requires hands-on clinical skills and site operations knowledge, with opportunities for professional development in clinical research.
What they're looking for
- 1–3 years clinical research experience at investigative site (CRC I) or 3+ years (CRC II)
- Proficiency obtaining vital signs, phlebotomy, ECGs, and lab specimen processing
- Demonstrated experience with pediatric blood draws
- Understanding of site operations and drug development process
- Strong written and verbal communication with attention to detail
- Proficiency with CTMS, eCRFs, and Microsoft Office applications
What you'll be doing
- Manage 2–6 concurrent trials of varying complexity from initiation to completion
- Recruit study participants and obtain informed consent per protocol requirements
- Perform clinical procedures and maintain regulatory documentation
- Coordinate with investigators, sponsors, and study monitors on trial activities
- Mentor junior staff and contribute to internal training programs
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.