Listed on IQVIA’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
You will manage clinical trial contracts for research sites across North America, drafting agreements and negotiating terms independently while coordinating with internal teams to keep studies on track. This role suits someone with pharma or CRO experience who can handle contract timelines, compliance, and stakeholder communication in a remote position.
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
- 2+ years clinical research experience in CRO or pharma
- Direct contract and budget negotiation experience with sites
- Advanced English proficiency