At a Glance
- Tasks: Support clinical trial start-up and site activation activities with document management.
- Company: Join IQVIA, a leader in healthcare data and analytics.
- Benefits: Flexible remote work, competitive pay, and opportunities for professional growth.
- Other info: Collaborate with diverse teams in a dynamic and impactful environment.
- Why this job: Make a difference in healthcare by ensuring timely and compliant trial submissions.
- Qualifications: Experience in clinical trials and strong organisational skills.
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, working with sites and internal study teams to ensure timely, compliant submissions.
The candidate will manage documentation, timelines, and cross-functional collaboration to ensure Green Light readiness.
UK Site Activation Specialist - Remote Freelance in London employer: IQVIA, Inc.
At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation. Our commitment to employee growth is evident through continuous learning opportunities and the chance to work with cutting-edge technology in the heart of the healthcare industry. Join us in a role that not only challenges you but also allows you to make a meaningful impact on global health outcomes.
