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About the Role:
- Seeking an experienced Freelance Site Activation Specialist for UK clinical trial start-up.
- Primary focus on UK submission document collection, ICF adaptations, and regulatory support.
- Work closely with investigative sites and internal study teams.
Key Responsibilities:
- Collect, review, and prepare site and regulatory documentation for UK submissions.
- Support regulatory submission preparation and ICF adaptations.
- Maintain study tracking systems and timelines.
Requirements:
- Minimum 2–3 years’ experience in Site Activation or Regulatory Affairs.
- Strong experience with site document collection and review.
- Bachelor’s degree in Life Sciences or related field.
IQVIA
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We seek out diverse talent with a relentless commitment to innovation and impact.