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(such as, Development Operations, Pharmaceutical Sciences, Safety Risk Management, Regulatory), and external regulatory, industry, professional and academic organizations. Ensure that all study and project
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support Due Diligence assessments Acts as a reviewer of audit reports from outsourced or routine audits Assesses audit plans and quality metrics to identify potential areas of risk Actively supports
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the facility is in a clean, organized, and professional appearance. Areas include bio-hazard, quarantine, and rodent immunocompetent and immunodeficient areas. Train new hires on CCM policies and procedures and
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allocation and risk management. As Associate Director, your advanced knowledge of the principles and concepts of project management and comprehensive knowledge of other vaccine research and development
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/Site Care Partner for assigned studies at country level in accordance with the overall project plan, manages and maintains accurate country level plans (e.g. timelines, budget, risk and quality plans
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Why Patients Need You Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based
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of site risk NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Availability to travel regularly within country and region is required. Work Location Assignment:Remote - Field Based #LI-PFE #LI
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deliverables remain on target to meet internal and external deadlines. The GLL serves as the GLM primary point of contact for Labeling Team members (e.g. Regulatory Strategist, Safety Risk Lead, Functional Line
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Why Patients Need You Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based
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Why Patients Need You Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients.Our science and risk-based