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 role manages site coordination and regulatory documentation for clinical research studies, handling contracts, compliance tracking, and serving as the main contact between research sites and sponsors. It suits someone with clinical research experience who enjoys detailed administrative work and coordinating across multiple teams.
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
- Bachelor's degree in life sciences or related field
- 1–3 years of clinical research or relevant experience, or equivalent education and training
- 3 years of experience in a healthcare environment, or equivalent