Responsible for Oncology products clinical development, including strategic planning to transfer clinical research ideas into high quality clinical recommendations, study execution and medical monitoring to clinical trials to meet regulatory requirement and company SOP requirement

ClinicalTrials Co-chairsclinicalstudyteamandworkscollaborativelywithotherstudyteammembers. PointofaccountabilitytotheBUfordesign,conduct,interpretationandreportingofoneormoreclinical studies(orelementsofthosestudies). Providesclinicalandscientificexpertisetotheclinicaltrialstrategyandprotocoldevelopmentprocess, includingacquisitionofknowledgeofcompetitorproducts. ThroughapplicationofEnhancedClinicalTrialDesign(ECTD)/EnhancedQuantitativeDrugDevelopment (EQDD),ensuresthemostefficientclinicalprotocolsaredeveloped. Designs/writesclinicaltrialoutlines,protocolsandamendments,incollaborationwithinternalcontributors (e.g.statisticians,OutcomesResearch(OR)specialists,clinicalpharmacologists,clinicalproject managers,RegionalClinicalSiteLeads(RCSLs),marketaccesscolleagues,commercialdevelopment colleagues),internalexperts(e.g.clinicalprogramlead,globalclinicallead,globalclinicalstrategylead), andexternalexperts(e.g.investigators,keyopinionleaders,advisoryboardmembers);ensuresdesignis consistentwithobjectives.

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