Clinical Trial Manager

1 month ago


Uxbridge UK, London, United Kingdom HAYS Full time

Global Pharma are looking to recruit an experienced Clinical Study Manager with strong Oncology (ideally solid tumours) experience in Primary Analysis and data analysis in general - Familiar with PFS and OS analysis, imaging management in oncology Clinical trials, ePRO management

12 month initial contract - Hybrid role, Inscope



You will typically manage Phase I studies or other smaller studies. You will define and incorporate study logistics and study plans to accomplish clinical study objectives. You may also participate in strategic initiatives.

• Manages all components of small clinical studies, including Phase I studies.

• May lead/support contract research organization (CRO) and vendor selection and, where applicable, manages all interactions and deliverables from relevant CROs and vendors.

• Typically serves as the key operational contact providing oversight for the site evaluation, initiation, and close-out visits in addition to routine monitoring visits, either directly or through CROs.

• Defines and develops the study logistics and clinical study plan for assigned clinical studies.

• Manages study timelines, including documentation and communications.

• Participates in and manages project meetings and conference calls with CROs, other vendors and cross-functional teams.

• Contributes to SOP development and/or participates in special projects. Develops tools and processes that optimize project efficiencies and effectiveness.

• Provides input into study protocols and case report forms, authors informed consents, study plans, and presentations.

• Provides oversight of study sites/region and reviews routine regulatory documents to ensure that CROs are in compliance with protocols, regulatory requirements, SOPs, and monitoring plans.

• May be required to present at internal or external meetings (i.e., investigator meetings).

• Leads or otherwise assists in the preparation of safety, interim and final study reports, including resolving any data discrepancies.

• Proactively identifies potential operational challenges and collaborates with other Clinical Operations’ colleagues to provide solutions to ensure study execution remains on track to defined protocols, budgets and timelines.

• Ability to manage any component of full cycle study management, from start-up to close-out.

• Advanced knowledge of study management best practices and tools and has shown ability to apply these to improve study efficiencies and effectiveness.


Please send CV



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