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Pfizer

Global Development Lead, Late-Stage Oncology Clinical Development (Non MD)

Pfizer, Bothell, Washington, United States, 98021


Global Development Lead, Late-Stage Oncology Clinical Development (Non MD)

Locations: United States - Washington – Bothell, Europe - Any Pfizer Site, United States - California - La Jolla, United States - Pennsylvania - Collegeville, United States - New York - New York CityTime Type: Full timePosted on: Posted 2 Days AgoJob Requisition ID: 4923263ROLE SUMMARYThe Global Development Lead will be responsible for defining and executing on the development strategy of two assets at different development stages. Reporting to the Vice President, GYN/GI/Melanoma Therapeutic Area Head, the successful candidate should have demonstrated proficiency in leading and/or supporting development programs, cross-functional collaboration, and represent program(s) externally.ROLE RESPONSIBILITIESLead product specific Global Development TeamsServe as the subject matter expert on clinical issuesWork across the organization and on the cross-functional Global Development Team to lead, develop and execute the clinical development plan of TIVDAK in cervical cancer and another new molecular entity entering late-stage clinical development.Endorse clinical decisions in advance of GPT, senior management reviews or governance bodiesProvide oversight and management responsibilities of medical director(s)Accountable 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 designsServe 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 and presentation of study dataAccountable with safety for clinical evaluations and safety decisionsAccountable with clinical pharmacology for defining and identifying optimal dose and schedule selectionAccountable with regulatory for health authority interactionsMay participate in evaluating business development opportunitiesBASIC QUALIFICATIONSAdvanced degree with relevant clinical/industry experience (typically 4+ years).15+ years industry experience5+ years of experience leading diverse teamsPrior management responsibilities of medical directors or clinical scientistsPREFERRED QUALIFICATIONSPast Clinical practiceExperience across multiple phases of clinical development and across drug classes in oncologyExperience in leading NDA, BLA or MAAThe annual base salary for this position ranges from $226,200.00 to $377,000.00. 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. 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.Relocation assistance may be available based on business needs and/or eligibility.Sunshine ActPfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.EEO & Employment EligibilityPfizer 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.About Us

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