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development process, related to monitoring clinical trials, GCP, FDA, or country-specific regulatory environment Demonstrated success in prior scientific/technical/administrative roles Demonstrated experience
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confirm that continuity and contingency plans are current Review and manage site practices that differ from Pfizer practices and liaise with study management and Business Process Owners as needed Maintain
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scaling of innovative solutions across the organization - from pilot phases to full-scale implementation. Collaborate on the delivery process , leveraging agile methodologies and best practices
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