PE Global
Clinical Trial Manager
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Clinical Trials Manager - 12 Month Contract
PE Global is currently recruiting for a Clinical Trials Manager for an initial 12-month contract role with a leading multinational Biotech client based in Stockley Park – hybrid.
As a Clinical Trials Manager, you may manage a geographical region(s) of assigned clinical studies or multiple components of larger studies, including vendor oversight responsibilities. You will define and incorporate study logistics and study plans to accomplish clinical study objectives. You may also participate in strategic initiatives.
Job Responsibilities
- With guidance, may lead contract research organization (CRO) and vendor selection and, where applicable, manages regional interactions and deliverables from relevant CROs and vendors.
- Typically serves as the key operational contact for our studies; 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 or components thereof, including documentation and communications.
- Participates in and manages regional project meetings and conference calls with CROs, other vendors and cross-functional teams.
- Contributes to SOP development and/or participates in special projects if required. 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 as required.
- Provides oversight of study sites/region/vendor 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).
- Assists in the preparation of safety, interim and final study reports as needed, 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.
- Collaborates with other functions on how to best achieve their study goals and objectives and communicates cross-functionally to ensure project team goals are met.
- Assists in training new or less experienced colleagues, if required.
- Ensures own work complies with established practices, policies and processes, and any regulatory or other requirements.
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Requirements
- PharmD / PhD with 2+ years’ relevant clinical or related experience in life sciences.
- MA / MS with 3+ years’ relevant clinical or related experience in life sciences.
- BA / BS / RN with 3+ years’ relevant clinical or related experience in life sciences.
- Multiple years’ clinical or related experience in life sciences, including experience leading or managing less complex studies and project teams.
- Experience managing the work of external vendors.
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Knowledge & Other Requirements
- Demonstrated ability to be a fast learner.
- Demonstrated ability to be flexible and adaptable to change, to move between projects easily and provide support/expertise where needed.
- 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.
- Fully understands protocol requirements and effectively articulates and interprets these.
- Thorough knowledge of Food & Drug Administration (FDA), European Medicines Agency (EMA), and other applicable national regulations, International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines and Good Clinical Practice (GCP) governing the conduct of clinical studies.
- Familiar with standard medical / scientific terminology.
- Ability to communicate in a clear and concise manner.
- Ability to support a team-oriented, highly-matrixed environment.
- Ability to execute multiple tasks as assigned.
Interested candidates should submit an up to date CV.
Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK
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