Pfizer, S.A. de C.V
Obesity - Global Study Manager II (Sr. Manager)
Pfizer, S.A. de C.V, Hartford, Connecticut, United States,
Obesity - Global Study Manager II (Sr. Manager)
We’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 Research & Development serves as the beating heart of Pfizer's trailblazing product pipeline, the essence of our mission to bring life-changing medicines to the world.Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.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.What You Will Achieve
You will be part of Pfizer's medical team and manage
obesity
clinical studies. Your project management skills will be leveraged for planning, directing, creating and communicating timelines. You will ensure that the clinical studies are within time, budget and scope.Must have recent experience overseeing Obesity studies.As a Senior Manager, your advanced knowledge of the principles and concepts in the obesity disease area 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 in 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.It is your problem solving ability and patience that will make Pfizer ready to achieve new milestones and help patients across the globe.How You Will Achieve It
Develop 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 sub team in partnership with the Study Operations Manager.Work proactively with country offices 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 recommends 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.Qualifications
Must-Have
Recent experience overseeing Obesity studiesBachelor's Degree7+ years' experienceApplicable pharmaceutical industry experienceWorking knowledge of Good Clinical Practices, monitoring, clinical and regulatory operationsDemonstrated project management / leadership experienceAbility 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-Have
Master's degree.Broad based experience in clinical researchWork Location Assignment: Remote - Field BasedThe annual base salary for this position ranges from $109,400.00 to $182,300.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 15.0% 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.Relocation assistance may be available based on business needs and/or eligibility.EEO & 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, 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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We’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 Research & Development serves as the beating heart of Pfizer's trailblazing product pipeline, the essence of our mission to bring life-changing medicines to the world.Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.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.What You Will Achieve
You will be part of Pfizer's medical team and manage
obesity
clinical studies. Your project management skills will be leveraged for planning, directing, creating and communicating timelines. You will ensure that the clinical studies are within time, budget and scope.Must have recent experience overseeing Obesity studies.As a Senior Manager, your advanced knowledge of the principles and concepts in the obesity disease area 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 in 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.It is your problem solving ability and patience that will make Pfizer ready to achieve new milestones and help patients across the globe.How You Will Achieve It
Develop 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 sub team in partnership with the Study Operations Manager.Work proactively with country offices 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 recommends 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.Qualifications
Must-Have
Recent experience overseeing Obesity studiesBachelor's Degree7+ years' experienceApplicable pharmaceutical industry experienceWorking knowledge of Good Clinical Practices, monitoring, clinical and regulatory operationsDemonstrated project management / leadership experienceAbility 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-Have
Master's degree.Broad based experience in clinical researchWork Location Assignment: Remote - Field BasedThe annual base salary for this position ranges from $109,400.00 to $182,300.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 15.0% 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.Relocation assistance may be available based on business needs and/or eligibility.EEO & 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, 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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