Global medical director- sickle cell disease

Vor 5 Tagen


Zürich, Schweiz Pfizer Vollzeit

POSITION SUMMARYAs an integral member of the global Sickle Cell Disease team reporting to the Global Medical Affairs Team Lead Sickle Cell Disease you will contribute to the development of the global medical strategy and tactical execution for Sickle Cell Disease (SCD) focusing on Voxelotor.KEY RESPONSIBILITIESWork closely with cross‑functional colleagues from Medical Affairs, Global Product Development, Biostatistics, Regulatory Affairs, Safety, Commercial and Market Access to ensure that the Sickle Cell Disease (SCD) global medical strategy/tactical and evidence generation plans with a primary focus on Voxelotor optimally address current and future needs.Lead the Voxelotor publications subcommittee and act as overall SCD publication lead to plan and implement appropriate publication strategies and tactics in accordance with Pfizer policy.Work with the publication process including concept author and agency liaison publications subcommittee review and allowing for promotional use if appropriate.Establish how the medicines profile fits into customer needs and the commercial strategy and compares to competitive medicines effectively communicating same to various stakeholders including patients.Development review and approval of internal and external medical materials; review and approval of commercial materials training of medical and XFT colleagues.Lead support and coordinate external medical communication initiatives via symposia proactive/reactive medical communication etc.Collaborate with colleagues in Medical Affairs to ensure all communications are aligned with the medical strategy with the patient at the heart of everything we do.Partner with Patient Advocacy to develop research studies to understand the patient and caregiver perspective around burden of disease and treatment outcomes.Partner with Global Access Strategy & Pricing colleagues to prepare reimbursement dossiers as appropriate.Contribute to GMAT and GMAT sub‑committees (Evidence Generation; Medical Insight and Impact; Medical Engagement) as appropriate.Collaborate with external study investigators, patient groups and other consortia to maximize synergies in development of and access to complementary data.Proactively bring patients & physicians voice to medical affairs efforts on cross‑functional teams while considering the needs of SCD providers and payers.Participate in the ongoing assessment of the benefit‑risk of the medicines taking into



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