At a Glance
- Tasks: Support clinical trial start-up and site activation activities across the UK.
- Company: Join IQVIA, a leader in healthcare data and analytics.
- Benefits: Flexible freelance role with competitive pay and the chance to work on impactful projects.
- Other info: Opportunity to work remotely and manage your own schedule.
- Why this job: Make a difference in clinical trials while collaborating with top professionals.
- Qualifications: Experience in site activation and regulatory submissions is essential.
The predicted salary is between 63000 - 77000 £ per year.
IQVIA is seeking an experienced Freelance Site Activation Specialist based in the United Kingdom to support clinical trial start-up and site activation activities. The role focuses on UK submission document collection, site document review, ICF adaptations, and regulatory submission support to ensure timely, compliant submissions.
You will collaborate with investigative sites and internal study teams to maintain quality submission packages, manage timelines, and ensure regulatory readiness.
Freelance UK Site Activation Specialist in Oxford employer: IQVIA Argentina
IQVIA is an excellent employer that fosters a collaborative and innovative work culture, providing its employees with the opportunity to grow professionally while working on impactful financial reporting across Europe. With a strong emphasis on employee development and proficiency in leading financial systems like PeopleSoft and SAP, team members can expect meaningful career advancement in a supportive environment that values integrity and excellence.
