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the acquisition and divestiture of TMF contentwhile developing repeatable efficient process for TMF in integrations Lead design and execution of remediation projects and improvement projects Configure Study
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, approaches of different reimbursement bodies) and lead the data generation process in countries in alignment with these. Excellent verbal and written communication skills including scientific writing skills
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programs and HTA analysis, approaches of different reimbursement bodies) and lead the data generation process in countries in alignment with these. Excellent verbal and written communication skills including
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of data and analytical solutions Lead the evaluation, implementation and deployment of emerging tools and analytic data engineering process in order to improve team productivity BASIC QUALIFICATIONS
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applicable SOPs and Business processes spanning Medicinal Sciences and Global Product Development (GPD) as required. Evaluate, propose and lead process enhancements efforts. Evaluate, propose and lead training
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ROLE SUMMARY: Lead as a player/coach the group of Asset Quality Leaders and accountable for the management and oversight of GCP performance and quality systems within the oncology portfolio
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function through engineering testing and Design Verification in support of product regulatory submission. The Principal Engineer position will also act as the Device Sub-Team lead and will be the Single
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assets or CD&O process area and drive learnings across their tumor type(s). Lead Level 1 quality review/assessment during Due Diligence and/or Integration activities. Oversee program and study-level
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strategic regulatory expertise as Global regulatory representative to Product Team(s). As a Director, Lead and coordinate a virtual global regulatory strategy team (GRST), encompassing regional regulatory
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As a member of a team of scientists in our In Vivo Pharmacology Cancer Cell Biology Group, you will play a lead role in using models of cancer to evaluate new drug candidates, mechanisms, and