Executive Director, Global Development Lead
2 months ago
This position is for an Executive Director, Global Development Lead within the GU Therapeutic Area.
The Global Development Lead will be responsible for defining and executing on the development strategy of Enfortumab vedotin. Reporting to the Vice President, GU Therapeutic Area Late-stage Development Head, the successful candidate should have demonstrated proficiency in leading and/or supporting development programs, cross-functional collaboration, and represent program(s) externally.
ROLE RESPONSIBILITIES
Work across the organization and on the cross-functional Global Development Team to lead, develop and execute the clinical development plan of Enfortumab vedotin in alignment with the Lifecycle Management Plan and Integrated Product PlanAccountable for the clinical development strategy, trial design, execution, and delivery of trial resultsAccountable for integrating regulatory, statistical and other internal and external stakeholder input into study designsLead product specific Global Development TeamServes as the subject matter expert on clinical issuesEndorses clinical development decisions in advance of GPT, senior management reviews or governance bodiesProvide oversight and management responsibilities of medical director(s)Serves as primary interface with Development Review CommitteeOversee the development and management of clinical protocols and amendments, investigator brochures, and clinical study reportsOversee the evaluation, interpretation, reporting, presentation and publication of study dataAccountable with safety for clinical evaluations and safety decisionsAccountable with clinical pharmacology for defining and identifying optimal dose and schedule selectionLeads the preparations of the clinical content of regulatory submissions/documents (e.g., NDA, MAA, IND, sNDA, IB, AR/DSRU, label changes, Core Data Sheet, Package Insert).Provides clinical input in the preparation and execution of meetings with health authorities, including leading discussions with regulators and leading/contributing to regulatory query responses.Supports business development initiatives, as appropriate, and as such may design/conduct/review protocols as a member of a due diligence team.
BASIC QUALIFICATIONS
Medical degree or advanced degree with relevant clinical/industry experience (typically 4+ years).7+ years industry experience5+ years of experience leading diverse teamsPrior management responsibilities of medical directors or clinical scientists
PREFERRED QUALIFICATIONS
Board certified/eligible in oncology or equivalentExperience across multiple phases of clinical development and across drug classes in oncologyExperience in leading NDA, BLA or MAA
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS
Ability to travel globally as needed.May be required to work outside of typical working hours to accommodate other time zones and address time sensitive business needs.
OTHER INFORMATION
Individual contributor or may have management responsibilities for 1-6 Associate Medical Directors, Medical Directors or Senior Medical Directors.Reports to Therapeutic Area Head
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.
Relocation support available
The annual base salary for this position ranges from $239,300.00 to $398, 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 | ). 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. This position requires permanent work authorization in the United States.
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