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The Associate AD - Governance and Regulatory Affairs provides leadership and oversight of the compliance, ethics and integrity program for the University of Wisconsin-Madison's Athletics Department.
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Reporting to the Director, Technical Writing, CMC Regulatory, CARGO is hiring a Senior Manager, Technical Writing to join the Technical (CMC) Regulatory writing function to help progress our cell-based gene therapy portfolio.
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Sr Director, CMC Regulatory Affairs –Small MoleculesKEY RESPONSIBILITIESThe Sr Director, CMC Regulatory Affairs for Small Molecules is responsible for managing a team of professionals, who work with Gilead’s global portfolio of small molecule products in CMC Regulatory Affairs.
$237,660 - $307,560ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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They will be responsible for strengthening awareness, affinity, and leadership of the Zoox brand, leading Media Relations, Public Affairs, Corporate Social Responsibility, Crisis Communications, Analyst Relations, and Event Activations.
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Partners with and provides subject matter expertise to key internal functions (regulatory, Quality, Clinical, CMC and formulations, Product Quality, Drug safety, Medical affairs) and their external contractors or collaborators.
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Camio already has a number of interesting case study customers, including Stanford University (DOD), Altria (regulatory compliance) and Delta Airlines (via NewRest/TSA for safety risk). Additionally, expertise in navigating complex regulatory landscapes and understanding the specific needs of governance, risk, and compliance applications would be valuable.
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You will need to work closely with the Vice President, Global Regulatory Affairs Oncology and Precision Medicine, and collaborate with the biomarker team and global/regional regulatory liaisons to provide Precision Medicine global regulatory guidance.
$205,700 - $266,200Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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SLAC National Accelerator Laboratory’s Office of Strategic Communications & External Affairs (SC&EA) is seeking an experienced Media Relations Lead to join the External Communications team. The Media Relations Lead will promote SLAC’s initiatives, research and people by writing, editing and distributing impactful press releases, crafting compelling media pitches, and organizing media events at SLAC. The Media Relations Lead will provide media training to SLAC staff and demonstrate critical leadership in dealing with sensitive media issues and crisis communications.
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Your primary responsibility will be to design, develop, and improve next generation sequencing (NGS) techniques to characterize CRISPR guide RNAs from research and development into a regulatory environment.
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Closely collaborates with various internal stakeholders such as Clinical Operations, Clinical Sciences, Regulatory Affairs, Biostatistics, Data Management, and Project Management, as well as external partners to ensure execution of pharmacovigilance activities in accordance with relevant regulatory requirements.
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The Senior Regulatory Affairs Specialist is responsible for developing strategies for global approvals to introduce new Spinal cord stimulation systems to market, maintain existing products, provide advice on regulatory requirements, prepare worldwide submissions, and negotiate their approval with global regulatory agencies.
$99,361 - $136,621 a yearFull-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Obtain Licenses: Become a FINRA (Financial Industry Regulatory Authority) Registered Representative by studying for and obtaining your SIE, Series 7 Top Off and Series 66 licenses, fully paid for and sponsored by Fidelity.
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Thorough understanding of clinical trial design and reporting processes, and regulatory reporting requirements including electronic data submissions, and CDISC implementation. Ensure quality of deliverables by consistently applying analysis and reporting standards and driving compliance with regulatory requirements, corporate, and departmental SOPs, and work practices.
$165,000 - $225,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Senior Regulatory Affairs Specialist, Redwood City, CA - Develop strategies for global approvals to introduce new Spinal cord stimulation systems to market, maintain existing products, provide advice on regulatory requirements, prepare worldwide submissions, and negotiate approval with global regulatory agencies.
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Be a UAS industry and regulatory/Part 107 SME to lead customers through training while ensuring compliance with FAA, state, and local guidelines. Bring a strong background in one technical area (examples: UAV systems, radio systems, software, security, prototyping, UI/UX design.
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regulatory affairs jobs Title: sr regulatory affairs associate Company: Thermo Fisher Scientific in Foster City, CA
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