Global Leukemia, Lymphoma and Biosimilars Medical Director (MD)
ROLE SUMMARY
The Global Leukemia, Lymphoma and Biosimilars Medical Director will be an integral member of the Hematology Cancer Global Medical Affairs Team. The Director combines the medical expertise and understanding of the patients’ and physicians’ point of view with that of the product/therapeutic area and is a part of a working environment where colleagues always understand and exhibit customer-focused medical professionalism with honor and integrity.
The Global Leukemia, Lymphoma and Biosimilars Medical Director will partner cross-functionally with Value & Evidence, Clinical Development, Legal, Compliance and Commercial colleagues to develop medical strategy and partner as appropriate to execute activities.
ROLE RESPONSIBILITIES
- Collaborate with a broad range of stakeholders to understand unmet medical needs and the therapeutic environment including the HCP and patient perspective, regulatory and access dynamics across regions and, integrate needs and insights to inform on-going Global Medical Strategy.
- Facilitate scientific engagement across a broad range of stakeholders to gain insight and increase understanding of the unmet need and treatment landscape in malignant haematology.
- Gather medical insights and translate them into actionable strategies focused on patients’ needs.
- Contribute to strategic evidence generation and dissemination plans.
- Support the execution of evidence generation activities including independent research, clinical and research collaborations, and Pfizer non-interventional and interventional studies including post-hoc data generation.
- Work on internal data interpretation and alignment activities.
- Support evidence dissemination and education activities including scientific publications and scientific exchange.
- Participate in and contribute to medical strategy governance teams.
- Develop/refine asset scientific narratives.
QUALIFICATIONS
BASIC QUALIFICATIONS
- MD/DO.
- 3 years relevant experience required. Medical Affairs experience preferred.
- Proven track record of ability to work successfully with cross-functional colleagues in a matrix team setting across countries and internationally with diverse colleagues.
- Well organized with the ability to prioritize and manage multiple demands while working independently.
- Very strong communication, interpersonal and relationship building capacity with demonstrated emotional intelligence and change agility.
- Strong strategic thinking and decision-making skills with the ability to translate country and regional insights and therapeutic area understanding into medical plans and strategies.
- Ability to assimilate large amount of complex data from diverse sources to convey complex concepts to non-scientific colleagues.
- Ability to influence without authority.
- Fluency in written and spoken English.
PREFERRED QUALIFICATIONS
- Clinical and disease knowledge base in malignant Haematology strongly preferred.
- International experience a plus.
- Global experience a plus.
- Regulatory and/or clinical development experience a plus.
The annual base salary for this position ranges from $205,400.00 to $342,400.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 25.0% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage.
Relocation assistance may be available based on business needs and/or eligibility.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
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