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Scientific Affairs & Regulatory Affairs. The Sr. Scientist II will execute the Scientific Affairs Strategy for your respective categories and geographical area using your Scientific and Regulatory expertise.
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Firm Type: Law Firm, Experience: 4 Years, A law firm is seeking a Securities Litigation Associate Attorney to join their team in Florham Park, NJ. The ideal candidate will have 4-6 years of substantive experience in securities litigation and regulatory practice, working on a variety of matters, including arbitrations, regulatory enforcement actions, and compliance issues.
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With 5 years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience. Job Title: Regulatory Studio - Associate Director, Precision Medicine & Digital Health.
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Working effectively with all cross-functional internal partners including HH, our Research & Development Division, Medical Affairs, Market Access, Regulatory Affairs, Legal & Compliance, as well as external Diagnostic and technology partner companies to successfully deliver on precision medicine goals.
$285,800 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Partner with Drug Metabolism and Pharmacokinetic (DMPK) and Bioanalytical (BA) Subject Matter Experts (SMEs) to author, review and track regulatory documents. Understand the impact of DMPK/BA and interdependencies with other functional teams within the enterprise including Pharmacology, Toxicology, Clinical and Regulatory disciplines.
ExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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8+ years relevant experience in quality control, quality assurance, and regulatory affairs at a Class I or Class II medical device manufacturer. Coordinate and organize test data and clinical or scientific reviews in support of regulatory submissions.
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Interface effectively with all other BMS internal stakeholders: Global Medical Affairs functions and other departments, including Commercial, Clinical Research and Development, Regulatory Affairs, Managed Care, Pharmacovigilance, Market Access, Statistics, Translational Research/Development, Project Leadership, etc.
Full-timeExpandApply NowActive JobUpdated 29 days ago - UpvoteDownvoteShare Job
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The Associate Director, PED Policy & Best Practices, will cultivate strong partnerships internally to enable effective cross-functional collaboration with HEOR, Clinical, Regulatory, Biostatistics, Regulatory Policy & Intelligence, Government Affairs, and Market Access teams.
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On-Board Scientific is hiring a Nonclinical Regulatory Document and Scientific Writer based out of either New Brunswick, Lawrenceville or Summit, NJ! Qualifications: At minimum, a Bachelor’s degree in Chemistry, Biology or related science with a strong background in DMPK and BA including knowledge of the FDA GLPs. + years of Regulatory drug development experience Experience with CTD documents and nonclinical study reports for submission to global regulatory agencies.
$57.78 - $62.5Full-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Collaborate with regulatory affairs and quality assurance teams to ensure compliance with submission guidelines and standards. Deep understanding of CDISC standards and regulatory submission requirements.
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Kept up to date on Digital Health technology regulatory requirements and worked on a digital pathology or digital health product in a drug. " Leadership responsibility for global regulatory strategy to support the development of biomarkers, companion diagnostic tests, digital health and other devices to enhance the value of our pharmaceutical products across therapeutic areas.
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As a member of the Risk & Regulatory Advisory team, you will advise financial institutions on a broad range of credit risk management topics including organization and governance; credit process optimization; risk rating model design, build and implementation; credit regulatory assessments; and Current Expected Credit Losses (CECL) process and tools.
$232,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Veteran Affairs, Intercultural Resource Center, Residence Life, International Student & Scholar Services, Community Standards, CARE Team, and Communications and will oversee the administration of budgets across all departments.
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Provide scientific and medical expertise to cross-functional teams, including research and development, regulatory affairs, market access, and commercial teams. Ensure compliance with regulatory and ethical standards in all medical affairs activities.
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Our client, a leading pharmaceutical company, is hiring a Nonclinical Regulatory Document and Scientific Writer, on a contract basis. The post Nonclinical Regulatory Document and Scientific Writer appeared first on TSR Consulting Services.
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regulatory affairs jobs Company: Mallinckrodt Pharmaceuticals in Summit, NJ
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