.Pfizer Executive Director, Global Development lead (Prostate Cancer) in Bothell, United States This position willbe responsible foroverseeing clinical trials and the development strategy for multiple medicines in prostate cancer.Reporting to the Vice President, Genitourinary Cancer Therapeutic Area Head, the successful candidate should havedemonstratedproficiencyin leading and supporting development programs across multiple functions within a company, as well as represent the program with the external clinical community.Lead, develop and execute the strategic development of therapies for multiple medicines in prostate cancerWork across the organization and on multifunctional teams responsible for the development of therapies for multiple medicines in prostate cancerLead product specific Global Development TeamOversee development for multiple medicines within a specificindicationor group of indicationsOversee the development and management of clinical protocols and amendments, investigator brochures, and clinical study reportsProvide oversight and direction to a team of medical directors and clinical scientists who lead the clinical study team for 1 or more medicines in prostate cancerOversee the evaluation of safety, pharmacology, and efficacy data from ongoing and completed studies medicines in prostate cancerOversee manuscripts, abstracts and presentations for scientific meetings and advisory boardsConduct literature reviews and prepare summaries to support clinical development programsMedical resource for design and interpretation of clinical and preclinical programs to support existing and new development candidatesLeads 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 responsesRequired Qualifications:MD, or,PharmD with BCOP certification and significant hospital-based experience, or, PA with substantial clinical oncology experience, or DO7+ years industry experience in oncology drug development5+ years' experience leading diverse teamsPreferred Qualifications:Has a strong leadership presence and the ability to work effectively with other clinical and scientific leadersDemonstrates a passion for helping patients with cancer and for the science of oncologyHas a collaborative style with internal company leadership, external development partners and investigators/medical professionalsIs a team player, works well in a team environment both as a leader and a key contributorHas a global perspective and mindset, with the ability to work effectively with colleagues from myriad cultures,backgroundsand geographiesSalary range listed is for the MD level only, other education level range can be provided during a screening call
