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Reporting to Head of Regulatory Affairs, the Senior Manager of Regulatory Affairs will support the day-to-day regulatory activities of assigned projects. Relevant (bio) pharmaceutical industry experience, including experience in regulatory affairs.
$169,000 - $195,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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In this role, you will be responsible for generating competitive intelligence, supporting our sales and public affairs teams, and providing technical expertise during customer, partner, and regulatory interactions.
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The Senior Product and Regulatory Counsel role is responsible for supporting the day-to-day business activities and legal requirements of the investment management and financial advisory, and broker-dealer products offered by Arta. Reporting into the General Counsel and working closely with the Compliance and Product teams, you’ll be responsible for shaping the development, launch, and growth of a portfolio of products aimed at modernizing equities investing.
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Job title: Regulatory Affairs Project Manager/Project Manager I. Regulatory operations: BUDI number updates, label reviews, FDA laser report, state manufacturing license etc. New product development documentation - On market support: regulatory impact assessments, etc.
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You’ll report to the Head of Corporate Affairs and work closely with GM’s Chief Trust and Privacy Officer as well as other executives. Lead communications and shape key decisions around privacy, cybersecurity, and safety as well as work on other key policy and regulatory issues.
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The Senior Medical Science Liaison (MSL) is a member of a field-based team of scientists who function as an extension of the US Medical Affairs organization. Collaborate with medical affairs and clinical organization to support patient enrollment in our company's sponsored clinical trials with site recommendations.
$168,000 - $252,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Public / Government Affairs: you have significant experience helping government organizations, or entities that work closely with governments, refine cyber security priorities and communicate clearly about these priorities.
$90,000 - $135,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Manager works collaboratively in partnership with Clinical and Regulatory Affairs to advance Shockwave Medical products. Partner within Clinical Affairs to streamline metrics related to clinical study execution and refine clinical data review processes to ensure oversight of clinical studies.
$129,000 - $191,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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This role requires strong collaboration skills and partnership with R&D, Global Strategic Marketing, Regulatory Affairs, Clinical Engineering, Supply Chain, Quality and Finance. Operates as the cross functional technical leader of the program with strong expertise in all aspects of large releases for complex capital equipment development (including Supply Chain, Quality, Regulatory and Clinical.
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Reporting to the Dean of Student Affairs and Activities, the Administrative Assistant, Senior supports the Office of Student Affairs and Activities. Administrative Assistant, Senior (Student Affairs and Activities.
$6,462.97 - $8,683.91 a monthFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Demonstrated competency and experience supporting Regulatory, Medical, and Clinical Affairs teams to ensure compliance for our Life Science and MDx products and tools around human disease and genetics.
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The Director/Sr Regulatory Affairs will lead the overall CMC Regulatory strategy for Adverum’s gene therapy program/s. Manage the Regulatory Affairs (CMC) Strategy for Regulatory Affairs.
$250Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Oncology Medical Director - MRD is a member of the Medical Affairs team and is both a leader of and participant on internal cross-functional program teams and working groups including, but not limited to, members of the business development, pathology and clinical lab operations, biostatistics, clinical affairs, regulatory, market access, and commercial teams.
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The Associate Director, Regulatory Affairs will be responsible for developing and implementing global regulatory strategies encompassing clinical, non-clinical and CMC disciplines.
$190,000 - $215,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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A "disabled veteran" is one of the following: a veteran of the U.S. military, ground, naval or air service who is entitled to compensation (or who but for the receipt of military retired pay would be entitled to compensation) under laws administered by the Secretary of Veterans Affairs; or a person who was discharged or released from active duty because of a service-connected disability.
$204,000 - $240,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago
affairs job Title: regulatory affairs Company: Thermo Fisher Scientific in Los Altos, CA
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