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Medical Affairs Director

2 months ago


London, Greater London, United Kingdom Novartis Farmacéutica Full time
About the Role

Job Summary:

We are seeking a highly skilled Medical Affairs Director to lead our Global Medical Affairs team in developing and executing medical affairs strategy for Hematology priority programs. The successful candidate will be responsible for leading the development and execution of medical affairs strategy, including transformative tactics such as research/population health, innovative partnerships, and integrated evidence plans.

Key Responsibilities:

  • Develop and execute medical affairs strategy for Hematology priority programs, including 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.
  • Partner with Development, S&G, US and International cross-functions to shape portfolio early and diversify evidence to achieve broad access at launch and to enhance impact on clinical practice for priority programs.
  • 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.
  • Represent 'the voice of the patient' internally and evaluate factors relevant to a patient's informed decision making.
  • Provide direction and input into the development and implementation of successful reimbursement and market-access strategies.
  • Provide proactive input to Development on potential new therapeutic indications, to enrich Registration Programs and to consider new therapeutic opportunities.
  • Ensure that Patient Access programs are supported for all brands within the GMA and delivered with full compliance.
  • Ensure 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.
  • Ensure that Patient Access programs are supported for all brands within International Medical Affairs and delivered with full compliance.
  • MD (Preferred) or PhD/PharmD in Health Sciences. Specialist Degree or specialist qualification related to discipline for which you will be responsible is an advantage.
  • 5+ years in Pharmaceutical Industry experience in Medical Affairs and/or Clinical Development.
  • Experience focused on studies - late studies, studies performance and being part of Clinical Research teams.
  • Experience on data and evidence generation.
  • Strategic mindset and ability to establish credibility and influence across a range of diverse stakeholders in a matrix organization to drive change. Project management and leadership (either direct or indirect) experience.
  • Highly preferred: experience and expertise in hematology, including launch and pre-launch activities, and clinical trials conduct.

Requirements:

  • MD (Preferred) or PhD/PharmD in Health Sciences.
  • 5+ years in Pharmaceutical Industry experience in Medical Affairs and/or Clinical Development.
  • Experience focused on studies - late studies, studies performance and being part of Clinical Research teams.
  • Experience on data and evidence generation.
  • Strategic mindset and ability to establish credibility and influence across a range of diverse stakeholders in a matrix organization to drive change. Project management and leadership (either direct or indirect) experience.
  • Highly preferred: experience and expertise in hematology, including launch and pre-launch activities, and clinical trials conduct.

Relocation: This role is based in London, United Kingdom or Barcelona, Spain. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.

Why Novartis?

Our purpose is to reimagine medicine to improve and extend people's lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us

Commitment to Diversity and Inclusion / EEO: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.