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environment with a cross-functional clinical team. BASIC QUALIFICATIONS PhD in Pharmacokinetics, Clinical Pharmacology, Pharmacometrics, Engineering or PharmD Strong written and verbal communication skills
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Quality Assurance, Medical Regulatory Compliance, R&D Legal, Corporate Compliance, Worldwide Safety & Regulatory and Pharmaceutical Sciences and other key study team members such as the Clinician, Clinical
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management as it relates to driving labeling process in regulated industry MS Office Suite; expert formatting skills (Word, XML) Bachelor's degree (in science or life sciences preferred) Attributes: Knowledge
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degree, preferably in a life science discipline. BS/BA +5 years, MS/MA +3 years, PhD +0 year s of experience in medical writing or related field. Understanding of the role of each member of cross
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PhD in Pharmacometrics, Clinical Pharmacology, Pharmacokinetics, Engineering, Pharmaceutical Sciences, or PharmD Strong written and verbal communication skills PREFERRED QUALIFICATIONS Experience
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advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply
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Why Patients Need You Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based
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ROLE SUMMARY As a member of our Oncology team, you will play a critical role in supporting Translational Science Operations strategies, through scientific technical oversight and management
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documents Facilitate team and cross functional meetings. Education Qualifications: Bachelor's degree in a science or life sciences required 3+ years experience in a regulated environment; pharmaceutical
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& Insights. The individual will interact with multiple cross functional team members within the SPP Centers of Excellence (COE), Pfizer Business Technology, Pfizer Incentive Comp team, Pfizer Business