Lead Clinical Delivery Programme Manager

1 month ago


Bracknell, Bracknell Forest, United Kingdom CK Group Full time £39 - £52
Programme Lead

CK Group are recruiting for a Programme Lead in Clinical Delivery, to join a leading pharmaceutical company in the industry, at their site based in the UK, on a contract basis for 12 months.

Role Overview
  • Lead the creation and execution of the exploratory and biopharmaceutics clinical development plans at a molecule level.
  • Technical leadership and operational oversight of clinical research trials within the development plan.
  • Responsible for planning and delivering exploratory and biopharmaceutics clinical molecules and submissions milestones on time and on budget throughout the molecule lifecycle.
  • Responsible for all aspects of global clinical trial operations within the plan.
  • You will be the single operational point of contact from trial design through execution and close out, including timeline creation and management, outsourcing plan, vendor management (including direct oversight of the operational deliverables), patient recruitment and retention and budget management.

Your Background
:
  • Bachelor's degree in a science related field from an accredited college or university.
  • 3-years' + experience in the pharmaceutical industry with direct experience of managing clinical studies, ideally in exploratory and biopharmaceutics clinical development (5+ year preferred).
  • Strong knowledge of regulations and guidelines that apply to the conduct of clinical trials.
  • Ability to influence and oversee TPOs to enable delivery of trial level deliverables.
  • Demonstrated knowledge and experience with project management tools and processes.
  • Demonstrated ability to work effectively cross-culturally and in a virtual work environment.
  • Demonstrated ability to influence both internal and external environments appropriately and forge strong working relationships.

Company
: A leading pharmaceutical company in the world, focusing on finding answers for some of the world's most urgent medical needs.

Location : This role is based at our client's site in the UK. You will be working 3 days in the office, and 2 days remotely. Requirements : It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

Responsibilities :
  • Lead the development of clinical trial plans and strategies.
  • Oversee the execution of clinical trials, including vendor management and patient recruitment.
  • Ensure compliance with regulatory requirements and industry guidelines.
  • Collaborate with cross-functional teams to deliver trial level deliverables.
  • Develop and manage project plans, timelines, and budgets.

Skills and Qualifications
:
  • Bachelor's degree in a science related field.
  • 3-years' + experience in the pharmaceutical industry with direct experience of managing clinical studies.
  • Strong knowledge of regulations and guidelines that apply to the conduct of clinical trials.
  • Ability to influence and oversee TPOs to enable delivery of trial level deliverables.
  • Demonstrated knowledge and experience with project management tools and processes.
  • Demonstrated ability to work effectively cross-culturally and in a virtual work environment.
  • Demonstrated ability to influence both internal and external environments appropriately and forge strong working relationships.


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