IQVIA
Freelance Site Activation Specialist (Study Start-Up / Regulatory Submissions)
- London
- Remote
- Freelance
Supports UK clinical trial start-up by collecting and reviewing site and regulatory documentation, preparing submission packages, and coordinating Informed Consent Form adaptations. Liaises with investigative sites and internal study teams to resolve outstanding documents and track progress against milestones, ensuring ICH-GCP and local regulatory compliance.