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content of regulatory guidelines and their interpretation in practice. Participate in research on statistical methodology and its applications pertinent to the Pfizer business needs. Help maintain a strong
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to achieve meaningful outcomes and create business impact. BS + 20+ Years relevant experience Global Regulatory affairs, Pharma QMS Development and Management, Clinical Quality, GCP Auditing, Regulatory
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, global CRO (project management, monitoring, regulatory affairs), and pharmacovigilance. Facilitate and oversee all national level regulatory filings for the trial(s). Collaborate with all relevant groups