Medical Director

2 weeks ago

London, Greater London, United Kingdom Russell Tobin Full time
About the Role

We are seeking a seasoned Medical Director to lead our Renal team. This 12-month contract will come with a competitive daily rate of £1,000.

The Global Medical Affairs team acts as the enterprise medical voice, leading medical strategy for therapeutic areas and developing Integrated Evidence Packages.

As a key member of our team, you will be responsible for implementing medical strategies for early programs globally, focusing on innovative evidence solutions, including interventional studies, NIS, RWE studies, and implementation science projects.

You will provide leadership and deep medical expertise in the TA, pivoting support based on business priorities and representing GMA with senior stakeholders when needed.

  • Lead development and execution of medical affairs strategy for Renal priority programs, including transformative tactics such as research/population health, innovative partnerships, and integrated evidence plans.
  • Co-develop plans for evidence generation, MSL/Field Medical Affairs strategy, medical education programs, scientific publication planning, and Medical Expert network development with TAs.
  • Co-own the development and implementation of innovative education and scientific communication plans for external stakeholders.
  • Financial tracking to ensure timely and cost-effective development & execution of medical activities.
  • Prepare SRC submissions for TA assets within remit.
  • Represent GMA around prioritized portfolio with internal and external audiences, in collaboration with TAs including the investment, medical and regulatory communities, as well as pharmaceutical or biotechnology industry collaborators/partners.
  • Provide direction and input into the development and implementation of successful reimbursement and market-access strategies.
  • Ensure that Patient Access programs are supported for all brands within the GMA and delivered with full compliance.
  • Ensures GMA activities are designed and executed in compliance with company policy guidelines and highest medical quality standards.
  • Provide proactive medical input to asset lifecycle management to consider new therapeutic opportunities.
Requirements

Must have:

  • MD (Preferred) or PhD/PharmD in Health Sciences.
  • 5+ years in Pharmaceutical Industry experience in Medical Affairs and/or Clinical Development.
  • Critical thinker with the ability to navigate uncertainty without major supervision.
  • Fluent oral and written English; Other relevant languages are an advantage.
  • Deep understanding of healthcare systems and key external stakeholders.
  • Strong track record of delivery focus for time and quality in medical affairs projects.
  • Successful development and implementation of innovative programs and processes.
  • Understands unmet medical needs, generates the right evidence to fulfill them, uses innovative, multichannel communication formats for effective evidence dissemination.
  • Agile mindset & ability to lead in an agile organization across Disease Areas.
  • Firm working knowledge of GCP, scientific and clinical methodology, protocol designs, management, and regulatory requirements for clinical studies designated for review by regulatory authorities.
  • Clinical trial research experience conducted in a pharmaceutical or equivalent academic environment in TA of interest is strongly desired.

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