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This role will support all commercial legal and healthcare compliance aspects of Kite’s cell therapy business in the U.S., including support for Commercial, Medical Affairs, Regulatory, Market Access, and Government / Public Affairs.
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Collaborate with other organizational departments responsible for functional aspects of the HIV Special Needs Plan, including, but not limited to Integrated Care Management, Behavioral Health, Managed Long-Term Care, Utilization Management, Quality Management, Credentialing, Regulatory Affairs, Compliance, Corporate Affairs, Provider Network Operations, Medicare Services, Information Systems, Finance, Claims, and Member Services and Eligibility.
$150,000 - $157,236 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Collaborate with cross-functional teams across Medical and scientific affairs, Data Science & Engineering, compliance, privacy, regulatory, IT, among others, to help shape and evolve the medical omnichannel solution roadmap and enhance evidence generation & dissemination strategies.
$113,000 - $170,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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You must be adept at cultivating strong collaborative relationships across Medical & Scientific Affairs as well as Infection Prevention & Control, Quality Affairs & Regulatory Affairs, Research & Development, Legal, and Health Care Compliance.
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Ability to assess R&D, non-clinical, and clinical documents for compliance to regulatory standards for GLP or GCP and to identify areas of non-compliance. We are seeking a highly motivated Regulatory Affairs and Quality Assurance (RA/ QA) experienced professional to join DermBiont.
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SRS provides financial reporting, regulatory compliance, and program management services to captive insurance companies. The successful candidates will have 5+ years of accounting experience working in the captive management industry to manage the financial and regulatory affairs of a portfolio of captive insurance companies.
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Participate as Global Product Strategy Lead in cross-functional teams, including but not limited to, contract research organizations (CROs), functional working groups, global regulatory team, submission team, product development team, to ensure compliance with regulatory requirements.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Regulatory Affairs Specialist IV. you will support Bio-Rad's commitment to quality and compliance by coordinating the Domestic and Intl Registration Requests as a Regulatory Specialist.
$107,200 - $147,400 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Collaborate with Quality teams to ensure compliance with regulatory standards, including but not limited to GMP, GLP, and GCP, as applicable. Lead and mentor a team of regulatory affairs professionals, fostering their growth and development.
$160,000 - $220,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Regulatory Compliance Expertise: Advanced understanding of local, state, and federal regulations related to underground utilities, coupled with the ability to effectively incorporate these regulations into permit drawings.
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The Senior Regulatory Affairs Specialist will provide regulatory support on a range of Endoscopy devices and activities which include new product introduction, evaluation of post market design changes, international submission support, commercial, manufacturing, & compliance support as well as other responsibilities aligned with global medical device regulations and goals of the business.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Foster strong relationships with cross-functional teams, including Marketing, Sales, Regulatory Affairs, Commercial Operations, and Medical Affairs, to align medical education strategies with company objectives.
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The AVP of Regulatory Affairs will be responsible for the planning, developing, directing, delivering, evaluating, and coordinating activities of the Regulatory Affairs Department.
$185,000 - $200,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Regulatory compliance competency including Quality Systems. Regulatory Affairs Certification (R.A.C) Develop and conduct training for internal and external stakeholders as needed to maintain compliance with evolving regulatory requirements.
$101,000 - $140,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Responsibilities Primary, direct legal counsel supporting activities related to one or more specific product franchises for the commercial, medical affairs, regulatory, and corporate communications functions.
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