Freelance Site Activation Specialist (Study Start-Up / Regulatory Submissions) – UK Remote
IQVIA · London, UK +4 more
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
This freelance position supports UK clinical trial start-up and site activation over approximately 3–6 months. Responsibilities include collecting and preparing regulatory documentation, adapting Informed Consent Forms, and liaising with investigative sites to ensure submission packages meet compliance standards. The role requires 2–3 years of experience in site activation, regulatory affairs, or clinical research, with a life sciences background and strong attention to detail.
Privacy & handoff
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