Medical Affairs Strategy Director

2 days ago

London, Greater London, United Kingdom Biocon Biologics Full time
Job Description

Biocon Biologics is a leading company in the biosimilars revolution, where patients come first. We are creating a model for the future of healthcare for all. Our ambition is to impact a billion lives by fostering a culture of affordable innovation, patient-centricity, and disruptive thinking. We are a multicultural global company where employees have a purpose and passion to work closely with partners and patients.

The Director Medical Affairs Strategy Europe will develop a differentiated Medical Affairs strategy tailored to the needs of the biosimilars environment for the European continent. This is a forward-looking and innovative role that will develop the opportunity space in Europe for a broad and expanding portfolio of biosimilar products. The role seeks to take Medical Affairs to the next level in terms of content and delivery.

The biosimilar environment offers unique aspects to be accounted for in a Medical Affairs strategy. This includes facilitating familiarity with, as well as confidence in the concept of bio-similarity. Furthermore, developing renewed interest in these products that have been with us for the most part for over a decade and recognizing the value they still represent despite potential new developments and incumbents.

The Director Medical Affairs Strategy Europe will report to the Chief Medical Officer. The role requires an open and curious mindset, a willingness to question the established and conventional way of considering the individual products and their established role in patient management, as well as taking a systems perspective on healthcare delivery across the European continent.

Responsibilities:

  • To curate a solid understanding of healthcare systems and the decision-making therein as it pertains to biosimilars in general and to individual biosimilar products in Europe.
  • Propose and develop projects and initiatives to leverage this understanding. Such projects may be educational in nature or research activities either in the form of desk research, or the development of explicit research proposals (database studies, observational research, etc.).
  • To develop and tailor a broad range of project proposals including cost-neutral activities that serve to highlight the merits of the biosimilar opportunity and the company-specific portfolio of products.
  • Draft and publish scientific manuscripts as they pertain to the biosimilar environment in general and/or specific aspects thereof in Europe. These may cover a wide range of topics depending on the opportunities identified, including real-world-evidence, health economics, clinical audits, and healthcare delivery research, case studies, and case series, etc.
  • Develop educational material and conduct educational sessions on topics pertinent to the biosimilar domain. Example topics include clinical perspectives on comparability exercises, comparative tolerability and safety - essentials in data interpretation, etc.
  • Develop a solid understanding of the products in the company portfolio and be able to apply this understanding to all other activities.
  • To work closely with the other members of the European and Global Medical Affairs teams to create synergies and efficiencies in meeting the overarching Medical Affairs mandate.
  • Collaborate constructively cross-functionally with all internal and external stakeholders with respect to the assigned responsibilities.

Qualifications:

  • Relevant academic qualification e.g. in the life sciences, e.g. Ph.D. or MD. Ideally able to convincingly entertain a clinical perspective.
  • Noteworthy experience that can be carried forward and qualifies for the role in terms of demonstrable scientific acumen, communicative skills, as well as strategic thinking and its translation into practical initiatives. The expectation is that the candidate has a track record that provides confidence in her/his ability to meet the requirements of the role.
  • The candidate is expected to be self-driven and to work independently and deliver on the entrusted activities. Set project goals are realised and implemented in collaboration with stakeholders. Progress reports are offered periodically.
  • Ability to critically appraise research in the clinical sciences field, including a relevant understanding of customary study methodology and statistical techniques.
  • Practical familiarity with the contemporary Medical Affairs environment, its practices, and the governing legislation and working knowledge of the compliance requirements.
  • A solid understanding of the European healthcare environment and its stakeholders including policy makers, advocacy groups, fundholders, and payors, etc. their respective interests and the issues they face as they pertain to the biosimilar domain.
  • A command of the English language that allows nuanced conversations and reflected written communication.
  • Professional fluency in at least one of the continental European languages.

Biocon Biologics is an Equal Opportunity, EEO / Affirmative Action Employer committed to excellence through diversity. All qualified applicants will receive consideration for employment without regard to, and no employee shall be discriminated against because of their race, color, religion, age, sex (including pregnancy), national origin, disability, genetic information, status as a protected veteran, or any other characteristic protected by applicable federal, state, or local law.

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