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developing and maintaining quality programs, processes and procedures that ensure compliance with established standards and guidelines. In this role, you will manage and support the operational process and
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Sciences group by way of process improvement. Develop expertise navigating Pfizer compliance systems, registries (e.g. GDMS, pTMF, Clinical Trial Registries, etc.) and other study systems related
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in Medical Affairs experience required Knowledge and experience in Hemophilia/Hematology is preferred Basic understanding of the drug development process Basic knowledge of health care economics and
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