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The Director must understand the entire preclinical and early clinical product development pipeline including product optimization, preclinical scale-up, and manufacture and toxicology, regulatory affairs, and early human clinical trials.
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Create and foster a climate of teamwork and effective working relationships both within Regulatory Affairs and with our internal business partners: Quality, Marketing, Legal, New Product Innovation, Science & Technology, Professional Veterinary Affairs, Supply Chain, and others to achieve the synergy needed to effectively work as a team and promote the business.
$128,000 - $150,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This role will liaise between groups within the R&D organization (Assay Development, Discovery Research, Biologics Research, and sister Process Innovation and Development groups), R&D Quality Assurance, Procurement, Supplier Quality, Regulatory Affairs, site-level Operations, and outside suppliers/vendors.
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Interact closely with Customer Service, Service, Repair, Research and Development, Quality Assurance, Regulatory Affairs and Sales to facilitate required action.
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Ability to draft technical reports summarizing research findings related to product development, raw material evaluation, and quality issues. Development of new products, and improvement of existing products including grouts, mortars, curing and sealing compounds.
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The Studies Program aims to advance the discussion of American foreign policy and international affairs through its writing, publications, public outreach, and discussions. Foreign Affairs , the preeminent magazine on global issues, and provides up-to-date information about the world and U.S. foreign policy on its award-winning website, CFR.org.
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In this new role, you'll lead the development and direction of the People Analytics function, reporting directly to the Senior Director of People Operations and Total Rewards.
$160,000 - $180,000 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Our newsroom covers a range of topics, including public and higher education, health and human services, mental health, immigration and the border, politics and threats to democracy, urban affairs, as well as climate, energy and the environment.
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The Medical Director provides strategic development, planning, implementation and oversight of Phase IV clinical trial programs within the Medical Affairs department for products in the therapeutic area.
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Responsible for development, implementation and maintenance of the company’s global regulatory affairs department and strategy. Minimum 8-10 years of combined regulatory affairs experience in color cosmetics, both in domestic and international markets.
$130,000 - $150,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Collaborate with Research & Development, Scientific Affairs, and Laboratory staff in any way applicable to support Clinical Trials. Method Development / Validation Facilitate assay development, conduct instrument validations and implement new testing to meet the needs of clinical trials protocols, clients and regulatory requirements.
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Expertise in commercial healthcare and FDA regulatory law, specifically related to market access, pricing and price reporting, patient support, government contracting matters, and other laws and regulations related to the development and commercialization of pharmaceutical products.
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EXAMPLE RESPONSIBILITIES: Represents Regulatory Affairs precision medicine subject matter expertise on cross-functional/cross-regional Regulatory Teams and other Sub-teams involved with the development and validation of IVDs (e.g., Study Management, Clinical, Biomarkers) and presents to senior leadership as required.
$205,700 - $266,200Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Director, Medical Research, is responsible for supporting strategic and operational activities of the Medical Affairs department and other functions at Intercept (e.g., R&D, Medical Safety) through real world evidence (RWE) generation.
$190,000 - $280,000 a yearFull-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Lead identification of assay requirements, lab selection, and contract development to ensure regulatory compliance according to GLP, GCP, and applicable global regulatory requirements such as CLIA and EU IVDR, and execution feasibility.
$200Full-timeExpandApply NowActive JobUpdated Today
regulatory affairs research and development jobs Title: medical director Company: Ecocareers
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