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productive working relationships with team members. Ability to collaborate with other medical writers across therapeutic areas for template or medical writing process creation/improvement. Extensive knowledge
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. Strong understanding of the drug development process and regulatory submissions. Proficiency in Microsoft Office applications (Word, PowerPoint) and collaborative authoring tools (Endpoint, Starting Point
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regulations Independently conducts wide range of routine/(non-routine) complex investigator site audits (minimal to no oversight - as needed) Executes audit strategy, leads/supports process audits, and may
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cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. ROLE SUMMARY This position will provide statistical support for
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ROLE SUMMARY The Senior Manager, GMA, Migraine is an integral member of the Internal Medicine Global Medical Affairs Team. This individual will provide scientific/medical leadership and support to
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experience in Automation Engineering Experience with process controls equipment; design and debugging skills Broad understanding of systems architecture and operations, and related components Excellent project
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throughout the labeling review and approval process through notification to stakeholders in order to ensure that these documents are produced in a timely manner according to internal SOPs and external
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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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ROLE SUMMARY The Senior Manager, Clinical Scientist (CS) will provide medical and scientific study and project support for multiple, global, Phase 1-4 vaccine clinical studies in a clinical program
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, monitoring of Laboratory Information System, monitoring status of staff credentials, training, competencies and certification of equipment. Confers with Administration, Medical Director, Laboratory Director