Global Development Product Lead, Essential Brands (Vice President)

SUMMARY
The Essential Brands Global Development Product Lead is responsible for the strategic oversight and operational leadership of Pfizer's Essential Brands portfolio of maturing pharmaceutical assets. This role ensures high-quality execution of post-marketing activities, lifecycle management, and expansion initiatives, driving operational efficiencies and supporting sustained revenue.
What You Will Achieve
In this role, you will:

• Serve as the single point of accountability for Essential Brands across Oncology, ensuring consistency in structure, resourcing, and ways of working.

• Oversee all development commitments and studies through loss of exclusivity, including transition planning from development teams to Global Brands.

• Drive global marketing applications, label updates, and publications to expand the reach of Pfizer medicines worldwide in alignment with US and global commercialization strategies.

• Manage regulatory, access, and periodic reporting requirements; fulfill post-marketing commitments and ensure data disclosure to support brands.

• Identify and implement resource efficiencies, regularly report on operational improvements, and support revenue through extension of LOE, delay of revenue erosion, and COGs reduction.

• Maintain and grow partnerships with development partners, research collaborators, and investigator-sponsored trials.

• Lead a cross-functional team and coordinate with dedicated functional team members (e.g., regulatory, safety, clinical operations, commercial, marketing, biostatistics, legal/IP).

• Accountable for the creation of an integrated product strategy and delivery through milestones and decision points by leveraging cross functional teams, with the goal of leading to approvals and maximizing product value
• Regular updating and communication with Disease Area Head on key program metrics, milestones, and risks
• Accountable for working with the GPTs to deliver the R&D budget, at or below target, and managing opportunities for savings or re-distributions of funding across programs
• Partner with Oncology Commercial, BD & Commercial Development to valuate US/ex-US opportunities for investment and building Oncology leadership under the direction of the Disease Area Head
• Integrates regulatory and statistical input into clinical trial design
• Drives and implements short- and long-term project vision and strategy, while ensuring alignment across global functions in regards to strategy and direction. Communicate clear strategy to program team and functions and ensures that is reflected in the operation
• Accountable with regulatory for health authority interactions
• Drives talent acquisition among team members and within their sub-teams, including active selection and de-selection and performance management in conjunction with line managers of the core membership of the program team
• Accountable with safety for clinical evaluations and safety decisions
• Primary governance interface for OLT/OSGT
• Accountable with clinical pharmacology, for optimal dose and schedule selection
• Accountable for external input from advisory boards and steering committees into clinical trial design
• Communicates with leadership and governance committees to address program needs, issues, resources, and recommendations. Ensures that presentations and other product communications are clear and effective. Support development of internal and external presentations.
• Drives team objective setting, prioritization and ensure adherence to Disease Area and overarching Oncology plan and strategy
• Drives risk management, issue identification and resolution and contingency planning
• Create a positive team environment that instills trust, encourages challenging assumptions, and ensures clear transparent communications to align around the overall goal/vision for the product

Here Is What You Need (Minimum Requirements)

• MD with minimum of 10 years of relevant experience in the pharmaceutical, academic, and/or medical research environments

• Demonstrated experience working on early and late-stage product development programs including regulatory filings (BLA/NDA, sBLAs/sNDAs), and product launches/life cycle management is strongly preferred
• Proven ability to lead and influence data-driven strategy planning and implementation
• A proactive and strategic thinker, with strong decision-making skills
• Experience working with corporate partners and alliance management
• Proven ability to function effectively across a matrix organization with multiple stakeholders and constituents, with the ability and strength to focus a team to work towards its goals
• Strong leadership and communication skills (including presentation skills) with success in influencing all levels cross-functionally
• Excellent business acumen with demonstrated ability to align teams to corporate strategy to achieve business and project objectives
• Strong staff management and mentoring experience and skills
• Highly collaborative with outstanding relationship building skills
• Experience in Oncology is required

The annual base salary for this position ranges from $295,900.00 to $493,100.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 30.0% 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. 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
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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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Medical