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 the activation and ongoing maintenance of clinical trial sites across multiple regions, handling regulatory strategy, documentation, and stakeholder coordination from pre-award through study execution. It suits someone with substantial clinical research experience who can navigate complex regulatory requirements while leading cross-functional teams and maintaining sponsor relationships.
Our summary, not IQVIA’s wording. The full posting is on their site.
What they ask for
Required
- Bachelor's degree in life sciences or related field
- 7 years of relevant experience in clinical or scientific environment with international exposure
- Strong negotiation and communication skills
- Thorough understanding of regulated clinical trial environment
- In-depth knowledge of drug development process
- Proficiency with systems and technology
- Regulatory and/or technical writing skills
- Knowledge of GCP and ICH guidelines
- Leadership ability to mentor and coach others
- Financial management understanding for studies
Nice to have
- Equivalent combination of education and experience in lieu of exact degree requirement