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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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Provide regulatory guidance to PI's and Research Staff to support the successful submission of regulatory compliant materials that are approved by the IRB or IACUC as applicable. Review all IRB and/or IACUC submissions to verify the required documents include all necessary information to make regulatory decisions.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Southwest Territory Includes: North TX, CO, OK, KS, UT, IDServing as a field resource for The Medical Affairs Company (TMAC), the Clinical Trial Liaison (CTL), reporting as Early Clinical Liaison, will represent the Company’s Respiratory Clinical Development program.
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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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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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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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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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Work closely with colleagues in other functions, including Regulatory Affairs, Clinical Operations, and Patient Engagement. Be responsible for the successful execution of research protocols according to FDA regulations and GCP guidelines.
$150 an hourPart-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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This position reports to the Executive Director of MSLs. The MSL will have contact with internal colleagues in compliance, regulatory, pharmacovigilance, marketing, sales, research and development, medical science, medical information, market access, training, strategy and portfolio management, and HOVA. This internal collaboration is considered a fundamental and essential part of the position.
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Regulatory Affairs Specialist provides regulatory guidance, monitoring and administrative help to the Institutional Review Board, Institutional Animal Care and Use Committee and Data and Safety Monitoring Board and other people involved in the conduct of research at all Baylor Scott & White Health.
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As a Senior Regulatory Affairs Specialist, Medical Devices at Verily, you will work directly with other Regulatory Affairs team members, partners, and a team of experts from diverse fields (e.g., Biology, Chemistry, Physics, Electrical Engineering, Computer Science) to develop, manage and execute regulatory strategies to obtain market clearances for innovative medical device products.
$166,000 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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At least 8-10 years of relevant pharmaceutical/biotechnology experience in R&D, including at least 5 years of relevant Regulatory Affairs experience (regional and/or global), in early development.
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Demonstrated knowledge and experience in Regulatory Affairs within the Oil & Gas industry. The role will involve working in Regulatory Affairs and will require an individual with a strong focus on reviewing and analyzing historical financial and operational records, particularly those related to assets.
$52 an hourExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Global system experience working with Regulatory Affairs Strategy, Intelligence, Regulatory Information Mgt & Operations, and/or Submission Publishing domains in support of market authorization.
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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.
$170,000 a yearFull-timeExpandApply NowActive JobUpdated 21 days ago
regulatory affairs jobs in Dallas, DC, Australia
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