$36,600 – $91,300
Listed on IQVIA’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This on-site clinical research coordinator role at an SMO offers hands-on experience managing multiple trials across different therapeutic areas, from patient recruitment through regulatory documentation. It suits someone looking to build broad expertise in trial operations while working closely with investigators and contributing to a collaborative team.
Our summary, not IQVIA’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- 1–3 years of clinical research experience at a clinical investigative site (CRC I level) or 3+ years as a Clinical Research Coordinator (CRC II level)
- Hands-on clinical skills including vital signs, phlebotomy, ECGs, and lab specimen processing
- Understanding of site operations and drug development process
- Strong written and verbal communication with attention to detail
Nice to have
- Mentoring experience with junior staff
- Experience with internal training contribution