Pfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes. Our mission is simple: empower healthcare decisions regarding the safe and appropriate use of medicines for patients.What You Will AchieveYou will be part of Pfizer's medical team and manage the clinical studies. Your project management skills will be leveraged for planning, directing, creating and communicating timelines while ensuring that the clinical studies are within time, budget, and scope.
As a Senior Manager, your advanced knowledge of the principles and concepts in the discipline and comprehensive knowledge of other disciplines will enable you to lead complex projects across the division. Your ability to develop and manage plans will facilitate achieving objectives, interpreting internal and external business challenges, and recommending best practices for improvements. While managing complex project environments, you will be able to anticipate and troubleshoot roadblocks and influence teams to achieve targets for the division.How You Will Achieve ItDevelop ideas, lead/co-lead complex projects across business units and develop plans to achieve objectives.Approve the Study Startup, Study Monitoring and protocol recruitment plans.Resolve escalated issues identified by the site activation subteam in partnership with the Study Manager.Work proactively with Clinical Research Organizations (CRO) and data management functions to ensure alignment on data flow and timely delivery.Manage Operational Study Management for one or more studies of limited complexity or a unique part of a larger study.Forecast and manage the Clinical Trial Budget for the program.Provide country and regional level input to country outreach surveys.Create awareness by working as a cross-functional Team Leader to deliver site intelligence initiatives with a variety of stakeholders, both internal and external.Approve and oversee drug supply management, manage flow of drug supply to the sites.Participate in global initiatives to improve operational efficiencies.Evaluate study progress reports and results for overall compliance and recommend corrective action or study termination for non-performance.Maintain regular communications with investigator sites to gather status updates, informal and formal performance metrics, and study-level feedback.QualificationsMust-HaveBachelor's Degree7+ years' experienceApplicable pharmaceutical industry experienceWorking knowledge of Good Clinical Practices, monitoring, clinical and regulatory operationsDemonstrated project management/leadership experienceExperience with CRO oversightAbility to evaluate, interpret, and present complex issues and data to support riskExcellent communication skills, both written and verbal; must be fluent in EnglishEffective decision maker, analytical and solution-orientedProficiency in Microsoft Office SuiteNice-to-HaveMaster's degree.Broad based experience in clinical researchStrong knowledge of Therapeutic Area, subject matter expertise, and international experienceLast date to apply: Aug 19th
EEO (Equal Employment Opportunity) & 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, or disability.
About UsPfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare and the potential to transform millions of lives. We're looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place.
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