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Clinical Trial Manager
2 months ago
Job Title: Clinical Trial Manager
Location: Remote (UK-based)
Job Type: Full-time, 12-month contract
Pay Rate: £420 - £440/day
i-Pharm Consulting is seeking an experienced Clinical Trial Manager to oversee the execution of Phase I - IV clinical trials across various therapeutic areas, with a focus on solid tumour oncology clinical trials.
Key Responsibilities:- Study Management: Oversee all aspects of small clinical studies, including Phase I trials, and manage multiple components of larger studies.
- CRO and Vendor Management: Lead the selection and management of Contract Research Organizations (CROs) and vendors, ensuring all deliverables are met.
- 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.
- Problem Solving: Identify potential operational challenges and collaborate with the team to provide solutions to keep studies on track.
- 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.
- Clinical Operations Expertise: Strong knowledge of study management best practices, GCP guidelines, and regulatory requirements (FDA, EMA, ICH).
- Communication Skills: Excellent ability to communicate clearly and work within a team-oriented environment.
About i-Pharm Consulting: We are a leading consulting firm specializing in pharmaceutical and life sciences projects. Our team of experts provides high-quality services to clients across the globe.
How to Apply: If you are a proactive Clinical Trial Manager with a passion for oncology clinical trials and a commitment to delivering high-quality data, please submit your CV outlining your qualifications and experience relevant to this role.
