Senior Director, Adult RSV Vaccine Medical Evidence Strategy Lead (non-MD)
Pfizer, New York, NY, United States
* 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, as indicated.* 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 trouble shooting major scientific/epidemiology issues during study implementation, including through travel to study sites when 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 of these manuscripts 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).* 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 as 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)* Direct experience overseeing post-authorization efficacy studies* Experience with adverse events assessments as part of vaccine effectiveness studies**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.Pfizer endeavors to make
accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@pfizer.com. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We’re looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place. #J-18808-Ljbffr
+ 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)* Direct experience overseeing post-authorization efficacy studies* Experience with adverse events assessments as part of vaccine effectiveness studies**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.Pfizer endeavors to make
accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@pfizer.com. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We’re looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place. #J-18808-Ljbffr