$44,300 – $110,500
Listed on IQVIA’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
A clinical research coordinator role at an SMO managing 2–6 concurrent trials, performing patient-facing clinical procedures, and handling regulatory documentation and study operations from recruitment through audit. This suits someone with 1–3 years of CRC experience who wants broad exposure across multiple therapeutic areas and a path toward operations or monitoring roles.
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 as Clinical Research Coordinator at a clinical investigative site (CRC I level) or 3+ years (CRC II level)
- Hands-on experience obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens
- Understanding of site operations and drug development process
- Strong written and verbal communication with attention to detail and time management
Nice to have
- Experience mentoring junior staff
- Contributing to internal training programs