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responsible for supporting VRD vaccine programs, has primary scientific responsibility in the evaluation of vaccine candidates. The incumbent is expected to develop, qualify, and transfer diagnostic and
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-budget execution of protocols Interact with regulatory authorities, key opinion leaders, and principal investigators. Leads Clinical Regulatory Authority interactions, accountable for providing responses
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or original ideas and lead business unit projects of a complex nature. Develop mid-term plans that impact the achievement of business unit results. Act as an enterprise leader in Quality, influencing and
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plans for own projects and leads small project teams. Monitor, generate and complete the periodic review, validation master plan for the automation engineering program. Demonstrate good planning
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, with a primary focus on integrated customers, including but not limited to National Payers, Regional Payers, and Specialty Pharmacy Providers (SPPs). The role is responsible for educating customers
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enrollment and study delivery timelines. The clinical study lead will be the primary liaison for investigators who have enrollment or extraordinary protocol issues that require escalation and may need
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with 8 years of experience OR a bachelors with at least 5 years of experience OR Masters Degree with more than 3 years of experience, OR a PhD with 0+ years of experience. 5+ years of demonstrated
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distilling complex analysis and concepts into concise business-focused takeaways. QUALIFICATIONS: • Bachelor's degree with 7+ years of experience OR Masters Degree with 6+ years of experience OR PhD with 2
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ROLE SUMMARY The successful candidate will join a team of ~45 scientists within the Primary Pharmacology Group (PPG) at our Groton, CT campus providing laboratory and automation support for tip
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technical aptitude, and creativity to foster original ideas are required for success in this position. CRD, as part of Pfizer R&D in Pharmaceutical Sciences, is responsible for the development of process