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Job Title: Clinical Trial Manager Work location: Monday to Friday, 37.Contract duration: A leading bio-pharmaceuticals company is looking for an experienced Clinical Trial Manager to join their Clinical Operations team This role involves overseeing the execution of Phase I - IV clinical trials across various therapeutic areas, with a particular focus on solid tumour oncology clinical trials, ensuring compliance with company policies, SOPs, and regulatory guidelines.
Manage Clinical Studies: Oversee all aspects of small clinical studies, including Phase I trials, and manage multiple components of larger studies.
Operational Oversight: Act as the key operational contact, providing oversight for site evaluation, initiation, monitoring, and close-out visits, either directly or through CROs.
Study Logistics and Planning: Develop study logistics and clinical study plans to achieve study objectives, including managing timelines, documentation, and communications.
Educational Background: PharmD/PhD with 2+ years, MA/MS with 3+ years, or BA/BS/RN with 5+ years of relevant clinical experience in life sciences.
Experience in Oncology Trials: Solid experience in solid tumour oncology clinical trials, and familiarity with PFS, OS analysis, imaging management, and ePRO.
Strong knowledge of study management best practices, GCP guidelines, and regulatory requirements (FDA, EMA, ICH).
If you are a proactive Clinical Trial Manager with a passion for oncology clinical trials and a commitment to delivering high-quality data, apply now to join our client's team and help drive the future of pharmaceuticals.
