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This position is a key leadership role for the development of the In Vivo franchise at CRISPR. Reporting to the Senior Director of Regulatory Affairs CMC, you will work closely with cross-functional teams and partners to bring multiple novel therapies to patients.
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We are seeking an Associate Director/Director, Regulatory Affairs, CMC to join our growing team. Associate Director/Director, Regulatory Affairs, CMC. This position reports to the Senior Director, Regulatory Affairs, CMC and will be in Boston, MA, USA. We will consider other jurisdictions for exceptional candidates.
$160,700 - $226,900 a yearFull-timeExpandApply NowActive JobUpdated 27 days ago - UpvoteDownvoteShare Job
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Reporting to the Sr. Director of Regulatory Affairs and Policy, this role will support and lead activities within the Regulatory group to advance development of the assets in Wave’s pipeline to registration and launch; will collaborate closely with team members within the group and across drug development disciplines such as CMC, Nonclinical, Clinical and Quality.
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The Associate Director, US Regulatory Affairs (RA) serves as the regulatory lead on relative Review Committees (RCs), for products in the Rare Disease, Rare Blood Disorder and Neurology portfolio.
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We are seeking an Associate Director/Director of Regulatory Affairs to join the company. Bachelor's degree in Biological Sciences, Pharmacy or related field is required; Advanced degree or certificate in regulatory affairs is preferred.
ExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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We're looking for an Associate Director Regulatory Affairs CMC , working in Pharmaceuticals and Medical Products industry in Cambridge, Massachusetts, United States. Manages timely regulatory submissions that involve CMC components including CTAs/INDs, NDA/MAA, and agency meeting packages.
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OPEN JOB: Pharma - Associate Director , US Advertising and Promotion , Global Regulatory Affairs - Hybrid. Represents Global Regulatory Affairs (US RA AdPromo) as a member of cross-functional brand and portfolio team review committees (RC), providing regulatory input into the review and approval of US advertising, promotion, disease-state, market access, and press materials.
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Proclinical is seeking an Associate Director, US Regulatory Affairs, Advertising & Promotion for a large global pharmaceutical company with locations in New Jersey and Massachusetts.
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The Training Associate Director is responsible for supporting the oversight of all Training related activities within the Global Regulatory Affairs organization. Manage Global Regulatory Affairs onboarding program, ensuring materials are kept up to date for optimal new hire experience.
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We are seeking a dedicated Regulatory Affairs and Quality Assurance Associate to join our team. Support regulatory filings including IDE, 510(k), PMA, and CE Mark applications.
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The Associate Director, Regulatory Affairs Advertising & Promotion will be responsible for providing strategic, operational and tactical regulatory advice to internal stakeholders regarding communications about investigational product pipeline assets and approved prescription products ensuring they comply with US laws and regulations and company policies, while supporting achievement of business objectives.
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Associate Director Global Regulatory Affairs CMC. At least 5 years professional experience in Global Regulatory Affairs CMC during clinical and/or registration for Biologics.
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0-3 years of experience in life science (pharmaceutical, biology, chemistry, bioinformatics) or engineering industry with a focus on information technology, clinical research, quality, regulatory affairs, manufacturing, or supply chain.
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Reporting to the Senior Vice President, Regulatory Affairs, the successful candidate will support the development of comprehensive regulatory strategies and collaborate with cross-functional teams to efficiently develop products in accordance with global regulations and guidelines.
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You will report to our Head of Regulatory Affairs and work side by side with your research and development colleagues to develop and execute innovative regulatory strategies for our development programs (from FIH through late-stage clinical programs), including the implementation of non-clinical and clinical regulatory strategy for relevant products.
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regulatory job Title: regulatory affairs associate in Melrose, MA
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