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D., Masters and Ph. D. preferably majoring in Pharmaceutics, Biochemistry, Molecular Biology, Biotechnology or Biology- RAC certification a plusExperience:- 7 years or more of CMC regulatory experience in the pharmaceutical industry with a history of successful of investigational filings and approvals of marketing applications as the CMC Regulatory lead.
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Basic Function HF Sinclair is seeking a Regulatory and Corporate Affairs Manager to support the Government Affairs and Corporate Management teams to further overall company objectives and identify regulatory and public policy trends.
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We invested in new offices, sector teams and practice groups including investor engagement; shareholder activism; governance; regulatory and public affairs, including geopolitical; crisis; litigation; social issues including climate change and diversity, equity and inclusion; cybersecurity, data and privacy; employee engagement; digital communications; opinion research and analysis, and creative services.
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Experience in managing regulatory relations or affairs in financial services, preferably including experience with the Federal Reserve and/or OCC. Serve as a key liaison between the bank and regulatory agencies, leveraging your prior expertise in regulatory relations or affairs.
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Preferred: Certification from the Society of Clinical Research Associates (SOCRA), Association of Clinical Research Professionals (ACRP), Research Administrators Certification Council (RACC), Certified IRB Professional (CIP) or Regulatory Affairs Certification (RAC.
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Your JobThe Product Safety & Regulatory Compliance Team is seeking a Regulatory Affairs Manager to join our team. Who You Are (Basic Qualifications)Experience working in regulatory compliance, chemical control, regulatory affairs, environmental, laboratory or product safety in the agriculture industry Experience working with chemical regulations Experience in the agricultural products / fertilizer industry.
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Job Description:AT&T is looking for a cybersecurity attorney to provide legal advice on a wide range of cybersecurity issues, including regulatory compliance, incident response, data protection, vulnerability management, and supply chain security.
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The Head, Real World Evidence will lead a team of RWE Scientists and work closely with cross-functional argenx teams, including HEOR, Clinical Development, Medical Affairs, Market Access, Commercial, Patient Advocacy, Business Development, Legal, Global Patient Safety, and Regulatory to align on the strategy for evidence generation efforts with identified evidence gaps.
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As our Regulatory Affairs Specialist, you will be joining our Health, Safety, Security, and Environment (HSSE) team and will be working closely with the Research and Development, Marketing, Operations and Sales groups.
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This position is part of Quality and Regulatory Affairs located in Fargo, ND and will be fully remote. The Director of Global Regulatory Affairs will be responsible for developing and executing regulatory strategies for drug development and commercialization ensuring compliance with global regulations and standards across multiple markets.
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Extensive interaction with departments outside of CMC Regulatory Affairs to define strategy and submission plans. An in-depth knowledge of ICH and regional CMC regulatory requirements, and an understanding of current global and regional trends in CMC Regulatory Affairs.
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The Pharmaceutical Regulatory Affairs Senior Manager will use their experience and knowledge in pharmaceutical industry regulatory affairs to lead and manage complex projects for our clients in the pharmaceutical sector, and provide strategic advice, guidance, and solutions on regulatory matters.
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Compliance and Regulatory Affairs: Ensure the company complies with all relevant laws and regulations in US, India, and Canada, including data protection laws, intellectual property laws, and industry-specific regulations.
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Since being founded the team has seen phenomenal and sustained organic growth, working across Medical Affairs, Publications, Promotional, Commercial and Regulatory spaces for their roster of blue-chip pharmaceutical companies and biotech's.
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UT Southwestern Medical Center is hiring for Immigration Specialist, Office of International Affairs Works to provide advisory, guidance, and administrative skills throughout several phases of immigration process in Office of International Affairs.
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regulatory affairs jobs in Dallas, WY, Ohio
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