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The Global Public Policy team's work spans a broad and diverse range of functions and workstreams, including government affairs and government relations; policy, product, and issue area expertise; risk and crisis management and mitigation; outreach, coalitions, and partnerships; and philanthropy.
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They will perform all required research related activities with IRB and regulatory affairs as well as oversee data entry and participant recruitment and enrollment. Expertise working with neurodevelopmental populations like autism, the person will have methodological expertise in data acquisition and analyses for neuroimaging (fMRI and high-density EEG), imaging genomics, and brain-behavioral task implementation.
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As a Senior Biologist/Ecologist, you will oversee and provide expertise in field biology, regulatory strategy, CEQA/NEPA analysis, and permitting strategy. Specific background and expertise should consist of strong botanical, wetland, or wildlife technical expertise, familiarity and experience with regulatory permitting, and project and client management.
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Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines.
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MedPro is one of the largest recruiters of therapists and nurses from outside the U.S. MedPro currently has contracts with numerous organizations to service a multitude of facilities in the U.S. The company counts among its clients prominent healthcare facilities and organizations such as the Department of Veterans Affairs,HCA, University of Miami Hospital, and Tenet Healthcare.
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The Biochemical Genetics Technical Director will be responsible for supporting the clinical, scientific, technical and regulatory aspects of the biochemical genetics laboratory. Familiar with regulatory and accreditation guidelines.
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May prepare and submit protocols, continuations/modifications, and related supporting documents to regulatory bodies such as the FDA, PPC, PRMC, IBCS (if needed), Cedars-Sinai IRB, Third Party IRB (WIRB) and any research committee involved in the Pre-Award/Post-award process.
$90,979.2 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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STGi is currently seeking a qualified Peer Support Specialist candidates for the Department of Housing and Urban Development (HUD) and Veterans Affairs (VA) Supportive Housing (HUD/VASH) Program.
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Familiarity with compliance and regulatory requirements related to social media marketing (e.g., GDPR, FTC guidelines) Audacy, Inc. (NYSE: AUD; OTC: AUDA) is a leading multi-platform audio content and entertainment company with the country's best collection of local music, news and sports brands, a premium podcast creator, major event producer, and digital innovator.
$150,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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POSITION SUMMARY: Under the supervision of the Program Director, provides recreational therapy and activities to Auerbach Geriatric Psychiatric Unit (AGPU) patients according to departmental, professional and regulatory standards of care.
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Public Information Officer/External Affairs. Public Information Officer/External Affairs. L952: All-Hazards Position Specific Public Information Officer. We continue to look for talented emergency management professionals to participate in our on-call response operations cadre in a ready status to provide staff augmentation to our client’s response and recovery missions.
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Monitor and advise Ed&IS and campus leadership on relations between UCLA and state, other governmental, and regulatory agencies, including but not limited to Community Care Licensing, California Department of Education Child Development Division, LAUP, and the National Association for the Education of Young Children (NAEYC), regarding child care licensing and regulatory matters.
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5 years, minimum, as in-house legal counsel (top-tier law firm candidates may be considered) advising on areas of law that impact multinational medical device companies such as intellectual property, compliance, commercial contracts, antitrust, privacy, healthcare fraud and abuse, FDA regulatory, corporate, and M&A.
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Familiarity with regulatory requirements related to reporting of child/elder abuse, substance use/abuse, child protective custody, adoptions, and other legal requirements. Familiarity with regulatory agency requirements, policies and protocols.
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Team with business unit Regulatory Affairs Specialists (RAS) to provide regulatory support for new product introduction (NPI) and marketed products under MDD and MDR Regulation. As Principal Regulatory Affairs Specialist, you will develop and implement medical device regulatory strategies to obtain timely approvals from worldwide regulatory bodies.
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regulatory affairs cmc jobs in Los Angeles, Columbia, Missouri
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