Senior Study Specialist – 6 months in scope hybrid role (London), 2 days on SiteThe Senior Study Specialist supports the delivery of clinical trials by overseeing study activities, vendor performance, and site operations. Working closely with the Study Manager or Programme Lead, you will help ensure studies arepleted on time, within budget, and inpliance with regulatory and quality standards.Key responsibilities include supporting study documentation, contributing to site feasibility and selection, overseeing CRO activities such as IRB/EC submissions, and managing essential documents across the study life cycle, maintaining Trial Master File (TMF) and coordinating meetings with internal teams and external partners.You will play a key role in vendor oversight, including monitoring performance, managing budgets and invoices, and resolving escalations. Also, contribute to risk identification and mitigation and support strong relationships with investigators and cross-functional teams.You ...