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 coordinates the setup and regulatory preparation for clinical research sites, acting as the main liaison between sites, project managers, and sponsors. It suits someone with clinical research experience who is organized, detail-oriented, and comfortable managing documentation and timelines across multiple studies.
Our summary, not IQVIA’s wording. The full posting is on their site.
What they ask for
Required
- Bachelor's degree in a related field
- 1 year of clinical research experience or equivalent education and training
- Knowledge of clinical systems, procedures, and corporate standards
- Knowledge of medical terminology and regulations
- Knowledge of clinical research processes
- Strong Microsoft Office and email skills
- Effective communication and interpersonal skills
- Ability to work independently and prioritize multiple tasks
- Attention to detail