Associate Study Start Up Manager

Job description

Associate 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: 4-6 months: Are you looking to take the next step in your Regulatory & Start‑Up career within clinical research? We are seeking an Associate Study Start‑Up Manager to support and deliver site activation, regulatory, and maintenance activities across clinical studies, working closely with cross‑functional teams and global stakeholders. This role offers the opportunity to build leadership capability, contribute to complex international studies, and play a critical role in bringing new therapies to patients. The Role: As an Associate Study Start-Up Manager you will support the delivery of site activation and maintenance activities for assigned studies or multi‑protocol programmes. You will help ensure regulatory submissions, contracts, and essential documents are managed compliantly and efficiently, while developing your leadership and project management experience. You will work as part of the study management team, contributing regulatory expertise throughout study start‑up and main...