Senior Clinical Project Manager - Cpl Life Sciences : Job Details

Senior: Clinical Project Manager

Location: Fully remote UK based

Contract length: 12 months FTC

Salary: 95 - 100k 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