Pfizer, S.A. de C.V
Global Development Lead, Late-Stage Oncology Clinical Development (Non MD)
Pfizer, S.A. de C.V, Groton, New York, United States,
Global Development Lead, Late-Stage Oncology Clinical Development (Non MD)
United States - Washington – BothellUnited States - New York - New York CityUnited States - Pennsylvania - CollegevilleUnited States - Massachusetts - CambridgeWe’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 offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.ROLE 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 TeamsServes 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.Endorses 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 designsServes 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. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). 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.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. 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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United States - Washington – BothellUnited States - New York - New York CityUnited States - Pennsylvania - CollegevilleUnited States - Massachusetts - CambridgeWe’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 offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.ROLE 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 TeamsServes 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.Endorses 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 designsServes 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. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). 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.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. 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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