We’re looking for an experienced Study Start‑Up Lead to drive efficient,pliant start‑up for clinical trials across the UK. Lead country start‑up strategy and site activation. Manage UK submissions (HRA, Ethics, MHRA) and amendments. Oversee ICFernance and site documentation, lead site contracting, budgets (iCT), and payment processes. Collaborate with cross‑functional teams, CROs & regulatory bodies. You must have strong experience in UK clinical study start‑up expertise with IRAS, CPMS, iCT, ARSAC Solid knowledge of ICH‑GCP, EU CTR, and UK regulatory processes.
Good Contracts negotiating and costing template experience
Proven ability to lead sites from set‑up to activation Excellentmunication and stakeholder management skills If you’re passionate about enabling high‑quality clinical trial delivery and want to make an impact, I’d love to connect. In scope, 6 month rolling hybrid contract, please send your CV to C
#4783908 - Claire Helliwell