Senior Clinical Project Manager

4 weeks ago


London, Greater London, United Kingdom Cpl Full time

Senior: Clinical Project Manager

Location: Fully remote UK based

Contract length: 12 months FTC

Salary: k per annum

Oncology experience: phase II - III

ASAP start

Cpl are working with a fantastic small growing Biotech now looking for a Senior Clinical Project Manager to join their team - please note: high flexibility is required and you must have worked on the sponsor side biotech/pharma

· Responsible for supporting the delivery of clinical studies ensuring quality and compliance.

· Responsible for clinical operations planning, oversight and execution of a clinical trial: responsible for overall timelines, budget and key deliverables

· Manage the operational execution of a clinical trial inclusive of all aspects of study conduct

· Participate on the clinical operations team and work closely with the medical team and other functional areas in support of the clinical strategy and development plan and in medical/operational execution of clinical trials

· Coordinate the day to day activities on a clinical trial both within the company and through a wide variety of CROs and vendors

· Provide clinical operations oversight and direction to both internal functional groups and external CROs/vendors to ensure trial goals and objectives are met on time and on budget

· Lead activities in the assessment and selection of CROs/vendors and participate in budget and contract negotiations

· Provide input and oversight in development of clinical plans, protocols, SAPs, consent forms and other study related documents

· Provide input in to, track, analyse and report performance metrics for each clinical trial

· Provide leadership/guidance to the study execution team and represent the clinical operations team in cross-functional team meetings

· Establish and manage relationships with CROs, vendors, investigators and other external partners

· Provide oversight for project -related data integration/technology activities including IVRS, ePRO, central lab etc

· Participate in discussions and help develop contingency/risk management plans for the clinical program

If this role is of interest please apply direct OR email your CV to



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