Senior Director, Adult RSV Vaccine Medical Evidence Strategy Lead (non-MD)

Senior Director, Adult RSV Vaccine Medical Evidence Strategy Lead (non-MD)

• Emerging Markets - Any Pfizer Site
• United States - New York - New York City

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding what we need to achieve for patients and how we will go about achieving those goals.

Pfizer Research & Development serves as the beating heart of Pfizer's trailblazing product pipeline, the essence of our mission to bring life-changing medicines to the world.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

ROLE RESPONSIBILITIES

• Ensure RSV adult studies are conducted appropriately in context of latest information on RSV disease, strategic goals of the program, and best practices in epidemiological methods.
• Design post-authorization epidemiology studies for RSV adult indication including assessments of post-licensure adult RSV vaccine effectiveness.
• Ensure methods and outcomes are harmonized across RSV adult evidence generation portfolio.
• Ensure all regulatory feedback on RSV adult VE studies is considered in future regulatory interactions.
• Execution of studies is done by another group within Pfizer, but role will provide technical oversight and coordination for those executing the studies to ensure design and strategic consistency across portfolio and be member of key study teams.
• Provide input on RSV adult study design and execution based on deep expertise in RSV disease and epidemiologic methods.
• Oversee the development of common strategies across studies and study sites, including common protocols, case report forms, and databases.
• Identify, establish, and maintain relationships with external partners that can collaborate with high priority global studies.
• Oversee aspects of study design (e.g., methodology, protocols, analytic plans) for high priority epidemiologic and other scientific studies.
• Provide expertise on vaccine safety concerns within context of RSV adult vaccine studies.
• Provide expertise in RSV diagnostics.
• Assist with troubleshooting major scientific/epidemiology issues during study implementation, including travel to study sites as appropriate.
• Work with internal and external experts in statistics and data analysis to analyze and interpret data from key RSV vaccine and burden studies.
• Work with internal and external experts to publish data in peer‑reviewed manuscripts, including taking the lead for writing the first draft if needed.
• Work with internal and external experts to develop abstracts and present data for scientific congresses, including taking the lead for writing and presenting in some cases.
• Develop strategy regarding the collection of epidemiologic and other scientific data in target regions necessary for enhancing RSV vaccine product labels.
• Take the lead in writing original manuscripts each year (such as conceptual manuscripts, position manuscripts, systematic reviews, or where appropriate manuscripts based on original data).

BASIC QUALIFICATIONS

• PhD with expertise in vaccinology and field-based and analytic epidemiology.
• At least 10 years of experience in vaccine-related or vaccine-preventable disease related medical/scientific activities including research, clinical development, epidemiological, and immunization programs.
• Recognized expert in vaccines and viral respiratory disease to be credible both internally and externally, evidenced by one or more of the following:
  • Lead or senior author of at least 5 peer‑reviewed publications or book chapters.
  • Principal or lead investigator for at least two major projects.
  • Presenting author for at least 5 abstracts at international scientific congresses.
• Specific expertise in adult RSV epidemiology and vaccine effectiveness studies.
• Demonstrated experience with participating in a matrixed team.
• Demonstrated ability to lead across diverse cultures and geographies.
• Significant cross‑functional leadership experience.
• Previous work experience on RSV disease considered a major plus but not required.
• Documented ability to manage projects to completion.
• Documented ability to take a relevant vaccine or vaccine‑preventable disease epidemiology project from start to end including conception, design, protocol, analytic plan, implementation, analysis, and reporting and interpretation of results.
• Ability to understand subtle issues related to RSV vaccinology and epidemiology.
• Able to review, evaluate, interpret, and present complex data; understand the emerging safety and efficacy profile of Pfizer RSV vaccines.
• Understand the critical data elements related to assessing the public health value of RSV vaccines, ability to oversee or conduct public health analyses of RSV vaccine impact, and ability to interpret data and data limitations for both Pfizer and competitor RSV vaccines.
• Proficiency with MS‑Office software (Word, Excel, PowerPoint).
• Excellent verbal and written communication skills including scientific writing skills as evidence by lead authorship in at least 5 peer‑reviewed publications in English.
• Strong interpersonal skills.
• Proven ability to influence and succeed through others and to form excellent relationships with key cross‑functional stakeholders.
• Demonstrated strong work ethic, and proven track record of delivering high quality within timelines.
• Willingness to travel (approximately 15% may be required).
• Fluent in English writing, reading, speaking.

PREFERRED QUALIFICATIONS

• Direct experience overseeing post‑authorization efficacy studies.
• Experience with adverse events assessments as part of vaccine effectiveness studies.

ORGANIZATIONAL RELATIONSHIPS

• Managerially, reports directly to the Team Lead, Medical Affairs, Adult RSV Vaccine Program; technically coordinates with RSV evidence generation staff scientific affairs.
• Participates at the global level with other colleagues in RSV vaccine program on issues of importance to global RSV epidemiology and vaccinology, with an emphasis on issues of relevance to RSV vaccine licensure, recommendations, and use.
• Coordinates activities with others working on RSV adult evidence generation including clinical scientists and medical evidence generation lead.
• Works closely with Pfizer country medical staff globally to ensure that studies are aligned with scientific, public health, and medical goals for adult RSV vaccines.
• Works with RSV KOLs globally.
• Define data gaps globally that will impede decision‑making related to RSV vaccine use, (including pre‑ and post‑licensure), prioritizing these gaps, and developing and implementing solutions to close these gaps.
• No direct supervisory responsibility.

PHYSICAL/MENTAL REQUIREMENTS

No specific physical or mental requirements.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Travel approximately 15% (up to 20%).

Work Location Assignment

This is a hybrid role requiring you to live within commuting distance and work on‑site an average of 2.5 days per week or more as needed.

Compensation and Benefits

The annual base salary for this position ranges from $230,900.00 to $384,800.00. 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. Pfizer offers comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.

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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