47 postdoctoral-position-in-material-science Manager positions at Pfizer in United States
Sort by
Refine Your Search
-
, including market research, data science, digital analytics, finance, and consulting. Our culture is about getting things done iteratively and rapidly, with open feedback and debate along the way. We believe
-
cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. POSITION SUMMARY As part of the Clinical Data Sciences (CDS) group
-
cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. POSITION SUMMARY As part of the Clinical Data Sciences (CDS) group
-
The Data Science & AI team with Commercial Analytics & AI (CAAI) organization is committed to transforming data into actionable intelligence, empowering Pfizer to stay competitive and innovative in
-
ROLE SUMMARY The overall role of the Early Clinical Sciences (ECS) Clinician is to support the development and execution of one or more studies for small molecule and novel biological therapies from
-
of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States. Engineering #LI-PFE
-
environment with a cross-functional clinical team. BASIC QUALIFICATIONS PhD in Pharmacokinetics, Clinical Pharmacology, Pharmacometrics, Engineering or PharmD Strong written and verbal communication skills
-
withstanding regulatory scrutiny. This position will focus primarily in Trial Master File Operations. Facilitate the execution of the TMF Operations' activities to enable complete, compliant and consistent study
-
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
-
related labeling documents e.g., for products within a similar class, of different dosage forms, and for generics. Set clear targets for review and approval timelines for labeling documents using effective