The Senior Manager, Global Labeling Lead (GLL) has overall accountability for the development and execution of global labeling strategy for their assigned products. This includes managing the end-to-end process of Target Labeling in early development, creation and maintenance of Core Data Sheets (CDS), and submission and label negotiations for US Prescribing Information (USPI), and EU Summary of Product Characteristics (EU SmPC). This role offers high visibility and the opportunity to work cross-functionally with SMEs, contribute to organizational strategic initiatives, and support Pfizer’s Oncology pipeline. The successful candidate should possess an eagerness to grow, an aptitude for strategic thinking, and a focus on delivering for patients.
Role Responsibilities
Lead the development, maintenance, and implementation of high quality labeling including CDS, USPIs, EU SmPCs, and patient labelingAuthor labeling content de novo based on scientific source data, understanding of regulations and guidance, and label precedentManage cross-functional Labeling Team and collaborate with stakeholders including Clinical, Medical, Safety, Regulatory, and CommercialDrive global labeling strategy through development of target labeling, scenario planning, and risk mitigationManage label negotiations with US FDA and EMAProvide guidance on labeling regulations, industry best practices, and competitor label assessmentsAct as the primary labeling representative on Global Regulatory Strategy Teams, Submission Working Groups, and other relevant product teamsContribute to strategic initiatives and process improvements across the organizationBasic Qualifications
Bachelor’s degree in a scientific or technical discipline.Minimum of 8 years of relevant labeling experience in the pharmaceutical or biotech industry.Advanced knowledge of external labeling guidelines and regulations.Ability to successfully understand regulatory implications of product strategy with regards to the product label, assessment and practical management of associated impacts.Preferred Qualifications
Oncology experience strongly preferred.Ability to develop strong and positive working relationships with cross-functional stakeholders and SMEs.Excellent written and verbal communication skills; complete fluency in English language.Proven strength in logical, analytical and writing ability.Strong project management skills and attention to detail.Proven ability to negotiate, influence and problem solve.
Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.
Work Location Assignment: This is a HYBRID role, requiring average 3 days onsite. Candidate must be within 50 miles of a Pfizer site (WA-SEATTLE, CA-SFO, CA-San Diego)
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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