Study Start-Up Manager

Job description

Study Start‑Up Manager Clinical Operations | Regulatory & Site Activation Location: Flexible / office‑based depending on project needs Travel: Occasional travel may be required Contract Length : 3- 6 months Are you an experienced Regulatory & Start‑Up professional looking to lead complex clinical trial start‑up activities across global or multi‑regional studies? We are seeking a Study Start‑Up Manager to take ownership of site activation, regulatory strategy, and ongoing site maintenance for high‑profile clinical research programmes. This is a key role within Clinical Operations, providing leadership, oversight, and subject‑matter expertise to ensure studies are delivered compliantly, efficiently, and on time. The Role: As Study Start‑Up Manager, you will direct and manage all site activation and regulatory activities for assigned studies or multi‑protocol programmes. You will act as a central point of contact for investigative sites, sponsors, and internal stakeholders, ensuring regulatory and contractual requirements are met throughout start‑up and maintenance phases. You will also contribute to business development and pre‑award activities , providing regulatory insight and solu...