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Pfizer

Makes cancer drugs, vaccines and other medicines

Global Medical Director - Respiratory

Biology & BiotechPosted on Nov 12
Full-timeNo salary listed

About the Job

Requirements

  • A relevant advanced scientific or clinical degree, such as an MD, PhD, or PharmD.
  • At least three years of pharmaceutical industry experience for candidates with an MD, or six years for candidates with a non-MD advanced degree.
  • Experience in Medical Affairs is required; global or above-country experience is preferred.
  • Demonstrated experience in evidence generation, evidence dissemination, data interpretation, and external scientific engagement.
  • Ability to work successfully with cross-functional colleagues in a global matrix and across countries and cultures.
  • Ability to guide colleagues and partners through influence without direct authority.
  • Experience translating strategy into executable plans and managing multiple priorities and dependencies.
  • Strong understanding of clinical development, study design, and the medical, regulatory, and access implications of scientific evidence.
  • Fluency in written and spoken English is required.
  • Ability to interpret complex clinical and scientific information and translate it into clear medical implications and actions.
  • Proficiency with standard business and collaboration software, including Microsoft Office applications.

Responsibilities

  • Demonstrate deep data, disease-area, and treatment-landscape expertise across assigned respiratory programs, including asthma, chronic obstructive pulmonary disease, and emerging respiratory indications.
  • Translate global Respiratory portfolio strategy into asset- and indication-level medical plans, clear priorities, deliverables, timelines, and success measures.
  • Ensure evidence-generation and dissemination strategies are developed and executed in alignment with the Respiratory scientific narrative, asset strategy, and priority objectives.
  • Lead insight-generation activities within assigned areas of responsibility through peer-to-peer interactions, field medical insights, advisory boards, scientific congresses, and literature surveillance, and translate insights into action.
  • Lead evidence-generation activities within assigned areas of responsibility, including defining the scope of independent research and designing clinical research collaborations, real-world evidence, and Pfizer-sponsored non-interventional or interventional studies in partnership with relevant platform functions.
  • Provide Medical Affairs input into development plans, pivotal-program readiness, clinical-trial concepts and protocols, endpoint strategy, data interpretation, and lifecycle planning.
  • Lead evidence dissemination and education activities, including scientific publications, congress presentations, scientific exchange, and internal medical education.
  • Lead development and execution of internal medical training curricula in collaboration with Medical Content and Communications and other platform functions.
  • Work closely with cross-functional asset teams to provide scientific and medical expertise across relevant workstreams, including target product profile development, differentiation, evidence priorities, and launch readiness.
  • Work closely with US, International, regional, and country medical colleagues to align global strategy with local insights and needs and support implementation of the scientific narrative and operating plans.
  • Build and maintain credible relationships with external experts, investigators, professional societies, collaborative research partners, and patient organizations, as appropriate.
  • Represent Global Medical Affairs on relevant asset, evidence, and cross-functional teams and ensure timely delivery of assigned medical milestones.
  • Identify execution risks, dependencies, and emerging opportunities; recommend mitigation or acceleration actions and escalate portfolio-level decisions to the Global Senior Medical Director.
  • Ensure all activities adhere to internal policies, applicable regulations, industry standards, and high ethical and scientific standards.
  • Lead cross-functional workstreams, guide colleagues and partners through influence, and oversee vendors, external research collaborations, and approved budgets associated with assigned medical plans, as applicable.

Desired Qualifications

  • Respiratory, allergy, immunology, or related therapeutic-area experience is strongly preferred.
  • Subject-matter expertise in asthma, chronic obstructive pulmonary disease, severe respiratory disease, biologics, or emerging respiratory indications is preferred; strong pipeline or launch experience in another relevant therapeutic area may be considered.
  • Launch, regulatory, clinical-development, real-world-evidence, or health-economics experience is a plus.

About the Company

Pfizer

Makes cancer drugs, vaccines and other medicines

Pfizer discovers, makes, and sells prescription medicines and vaccines for patients, doctors, and governments worldwide, with large businesses in vaccines, cancer, heart disease, and rare diseases. In 2020, its COVID-19 shot, developed with German partner BioNTech, became the first COVID-19 vaccine authorized in the United States. Its scientists find drug candidates and run clinical trials to prove they are safe and effective, and Pfizer then manufactures approved products in its own plants, earning most of its money from patented drugs before cheaper generic copies arrive. Pfizer was founded in 1849 as a chemicals business in Brooklyn and is based in New York City.

Company size
10,001+
Company stage
IPO
Headquarters
New York City, New York
Founded
1849

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