The Senior Medical Director will be responsible for leading several US Medical Affairs activities in support of Prostate Cancer, including but not limited to:

　　Provide deep expertise in prostate cancer disease state and treatment.

　　Provide deep expertise in biomarker testing & precision medicine.

　　Ensure US launch readiness for new assets/indications. Develop and execute short and long-term US Medical plans, aligned with overall business goals.

　　Work closely with Global Medical Affairs and other cross-functional colleagues, as appropriate, ensuring that the US Medical Affairs plan is aligned with brand strategies to support successful pre-launch, launch & post-launch medical initiatives.

　　Understand and integrate the needs/perspectives of patients and HCPs into Medical plans & tactics.

　　Responsible to lead strategic medical partnerships with key external organizations from a GU portfolio perspective

　　Strategic Medical leadership in ongoing sponsored study clinical research.

　　Responsible to oversee strategic fit and operational excellence of US ISRs from a GU portfolio perspective.

　　ROLE RESPONSIBILITIES

　　Brand Plan Development

　　Oversee and coordinate medical input into brand strategies and tactics, aligning on US regional medical needs.

　　Lead the development and timely execution of medical strategies and tactics.

　　Medical Sub-Team

　　Participate, as needed, on Medical sub-team meetings and activities.

　　Partnership with Global Medical Affairs to assure US is represented in Global Medical decisions and ensuring GLocal coordination in all activities.

　　Promotional Materials Review

　　Provide clear medical input on promotional and sales training materials, in partnership with Legal, Regulatory and Marketing colleagues, to ensure compliant, accurate, fair-balanced and high-quality content of all commercial materials.Customer Insight Planning

　　Provide leadership for the development and implementation of customer insight planning (including Advisory Boards) to gather expert guidance to advise medical planning.Research

　　Develop strategies and manage Investigator-Initiated Research program, Clinical Research Collaborations and analyses of Real World Data.

　　Develop and advocate for Phase IV lifecycle clinical trial strategies and concepts to support regional medical business needs

　　Publication Subcommittee (PSC) Membership

　　Collaborate with Global Scientific Communications and Clinical Development on key governance committee to support development of strategic global and regional publication plans.

　　Participate in data analysis efforts, and lead or participate in manuscript, abstract, and poster development.

　　Safety Support

　　Represent regional medical on internal safety committees, safety analysis and interpretation of clinical and RWD, guidance for safety updates, issues pertaining to regional business.

　　Regulatory Support: Provide regional medical leadership, support and guidance for new labels, label updates and responses to regulatory requests.

　　Customer Facing Partnerships

　　Partner with expert thought leaders and societies to support regional Medical business goals, including manuscript generation, research partnerships, fellowships, expert guidance, and competitive insight.

　　Provide primary medical leadership & support for regional medical congresses.

　　Leadership & Mentorship

　　Effective leadership within team matrix, excellent interpersonal skills.

　　Responsible for developing and coaching other team members as requested.

　　Support a high-functioning and performance culture for team

　　Subject Matter Expertise

　　Serve as a medical/clinical expert in the diagnosis and treatment of patients with prostate cancer to bring the voice of patients & physicians to efforts and initiativesQUALIFICATIONS

　　PhD, PharmD, DVM professional degree

　　8 or more years experience in either pharmaceutical industry, academic centers, clinical practice, or a combination of these.

　　Experienced in the diagnosis and treatment of patients with prostate cancer within the US Healthcare System.

　　Headquarters and launch experience strongly preferred.

　　Knowledge and experience in prostate cancer preferred.

　　Deep expertise in biomarker testing and precision medicine required.

　　Understanding of the drug development process & experience with efficiently managing investigator-initiated research

　　Knowledge of health care economics and its impact on medical decision making desired.

　　Highly motivated with demonstrated track record of high performance and excellence.

　　Strong strategic skills including creativity and effectiveness in proactively identifying and addressing challenges.

　　Strong interpersonal skills and excellent verbal communication and presentation skills. Proven ability to facilitate open discussion and debate among key stakeholders and build internal and external relationships.

　　Well-organized with the ability to be flexible, prioritize multiple demands, and effectively lead in a matrix organization.

　　PHYSICAL/MENTAL REQUIREMENTS

　　Capable of comprehending and communicating a large amount of scientific information in a clear & concise manner.NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

　　Ability to work flexible hours

　　Travel: 25%

　　ADDITIONAL DETAILS

　　Last date to apply for Job : February 10, 2024The annual base salary for this position ranges from $191,300.00 to $318,800.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 22.5% 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. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.

　　Relocation assistance may be available based on business needs and/or eligibility.

　　Sunshine Act

　　Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.

　　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.

　　Medical

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