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Reporting to the Regulatory Affairs Manager, the role involves collaborating closely with R&D, QA, and other departments to ensure compliance and support product development. The Regulatory Affairs Associate ensures regulatory clearance for all company products across all markets while maintaining compliance with all applicable regulations.
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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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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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We've placed hundreds of professionals including executives, managers, veterinarians, sales reps, and more in areas including professional services, research and development, pharmacovigilance, regulatory affairs, marketing, sales, etc.
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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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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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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.
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Our Company Gentiva Hospice is a member of the Gentiva family - an industry leader in hospice, palliative, home health, and personal home care. This role will manage budgets and ensure that organizational goals are in keeping with conscientious, humane care of patients while complying with all federal and state guidelines Knowledge of hospice operations, state and federal regulations and compliance.
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This administrative position will support the Conflicts of Interest and Export Control Offices within the Office of Research Regulatory Affairs. UT Southwestern Medical Center is hiring an Administrative Associate, Office of Research Regulatory Affairs.
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Our client in clinical trial studies is excited to share they are growing and looking for a new Principle Investigator in Gastroenterology. Be responsible for effective execution of research protocols according to FDA regulations and GCP guidelines.
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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.
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Participate in regulatory affairs, investigations, audits, and inquiries to uphold high standards. Job DescriptionJob DescriptionSenior Microbiologist Position at Synergy BioscienceAbout Us: Synergy Bioscience is a Contract Research Organization (CRO) that supports pharmaceutical, biotechnology, and medical device companies with product development, analytical chemistry, and microbiology testing services.
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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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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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Responsible for adhering to all legal, regulatory and HCC policies to including AdvaMed, Pharma, ACCME, Sunshine Act, etc. In collaboration with others in Office of Medical Affairs, works to ensure personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental compliance.
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regulatory affairs jobs in Dallas, East-hartford, Connecticut
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