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Clinical Project Manager

Zoek Pin Cambridge, Cambridgeshire, England


Permanent (Full time)

I’m working with a world renowned who are seeking a Clinical Project Manager to join the business on a 12 month contract.

Make sure to apply quickly in order to maximise your chances of being considered for an interview. Read the complete job description below.

This role will be responsible for all assigned studies

  • clinical operational oversight as well as the execution of monitoring of study deliverables, performing protocol-related site management activities, participating in study planning and set-up activities including vendor management, project management, coordination of study and implementation plans and supporting third party vendor relationships.

Role Responsibilities include: Responsible for the oversight and day-to-day management of clinical operations activities Ensure that the planning, implementation, coordination and reporting of the clinical studies in line with the corporate objectives Act as a key study contact for studies and effectively plan and communicate study milestones, deliverables, timelines and quality standards to other functions and other stakeholder groups Support and mentor team of Associate Clinical Project Managers/Clinical Trial Associates assigned to studies Support and monitor CRO and third-party vendor activities, including IMP management, Investigator contract/budgets, TMF management, study set-up, project management, biostatistics and medical writing Monitor progress of studies, identify study-related trends/issues and work with the Senior Clinical Operations team to implement corrective actions when necessary Attend site visits (including, but not limited to, Site Initiation Visits and study surgeries) where local and national travel policies allow Work with the study team to develop recruitment strategies Through adoption of a site centric model, liaise directly with assigned sites to ensure maintenance of site relationships, troubleshoot study related issues and impart key messaging to the site Drive the identification and selection of clinical trial investigators as per clinical operations strategy In conjunction with Surgical Technical Expert Liaison, oversee execution of the Surgical Training Plan Adopt a Risk Management approach to oversight and execution of assigned clinical studies Lead study operational and/or scientific feasibility, and site set-up activities as per clinical operations strategy Skills and Experience: Minimum 3 years’ experience working as a Clinical Project Manager in Phase I-IV studies within the pharmaceutical industry or a CRO Extensive experience in direct management of study start up activities Independent thinker with ability to anticipate issues and risks and to mitigate accordingly Team player who is able to prioritise workload in a fast-paced environment Working within a small to mid-sized Biotech Oncology / Biologics therapeutic experience would be ideal

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