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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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Develop, implement, and monitor procedures designed to promote compliance with IACUC policies and procedures and integration with other committees, such as the Institutional Review Board (IRB), Institutional Biosafety Committee (IBC), Chemical Safety Committee (CSC), and offices, such as the Sponsored Programs Administration (SPA), Office of Technology Development, and Legal Affairs.
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We’re a leader in staffing Clinical Development, Clinical Operations, Regulatory Affairs, Medical Affairs, HEOR, Market Access, and Sales & Marketing roles. Medical Science Liaison, Medical Device, Respiratory (Central) TMAC - Dallas, TX, United States Tagged: TMAC Direct Hire, Pharmaceutical, Medical Science Liaison, Respiratory, Field Medical , TMAC, Medical Affairs, MSL Medical Science Liaison, Medical Device, RespiratoryTwo Territories: Central and WestTMAC’s direct-hire service, formerly known as TMAC Direct, is an executive search firm and Pharma’s Complete Recruiting Resource.
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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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I have a talented group of recruiters who specifically source Technical Sales Professionals, Scientists, Regulatory Affairs, Scientific Affairs, Executive Technical professionals, Quality Assurance, Product Development, Technical Service, Nutrition, Analytical and Corporate Chefs.
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At least 5 years’ experience in regulatory affairs, clinical research, monitoring, data management, safety/pharmacovigilance, pharmacy, laboratory, or other relevant area in life science such as technology, third party supplier management.
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We invested in new offices, sectors and a wider variety of offers for clients such as public and regulatory affairs, major litigation, business and society, cyber, employee engagement and digital.
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Strong regulatory affairs and governance requirements for healthcare. Thorough knowledge of state and local guidelines that govern regulatory processes for healthcare. Strong regulatory affairs and governance requirements for healthcare.
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We are seeking a detail-oriented and analytical Business Analyst to join the Office of Research Regulatory Affairs. We are seeking a detail-oriented and analytical Business Analyst to join the Office of Research Regulatory Affairs.
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Effectively lead Cross-Functional/Cross-Community efforts (commercial, Tech Ops, medical affairs, market access, regulatory, R&D, etc.) Ensure PAPs are aligned with regulatory requirements, industry standards, and patient needs, optimizing program effectiveness and efficiency.
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Designs and delivers CRA, community development economic inclusion and other educational or marketing materials, either individually or in conjunction with other DCP regions, government and regulatory agencies, and private organizations, for the benefit of examiners, bankers, and community representatives.
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Currently seeking a new Global Director of Regulatory Affairs to help spearhead our client's 1st generation PMA submission as well as future supplements and OUS international registries for global commercialization.
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Engage with and lead advocacy efforts with regulators in Asia and EMEA on Public Cloud in partnership with Government Affairs and Regulatory Engagement teams. Strong understanding of cloud governance, risk assessment, and regulatory compliance in a multi-cloud environment.
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Leverage data to examine impacts to Customer Experience and Regulatory breaks. Risk certifications such as the CIA, CISSP, CISA, CRISC, CGEIT, CDPSE, etc. Negotiate with IA (Internal Audit; Third Line of Defense) and ORM (Operational Risk Management; Second Line of Defense), and with Policy Owners when more cloud-friendly policy changes need to be influenced.
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Minimum of 2-5 years related medical, regulatory affairs and/or research and development experience in the pharmaceutical, biotechnology, medical devices industry. Solid understanding of FDA, OIG, HIPAA, and other US regulatory.
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regulatory affairs jobs in Dallas, TX
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