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Piper Companies is currently seeking a Regulatory Affairs Specialist, Gene & Gene Therapy for an opportunity in Philadelphia, Pennsylvania (PA), to join an innovative biotechnology company creating life-saving cell therapies.
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Located within the Office of the Secretary, the incumbent will serve as an office manager for the Offices of Communications and Legislative Affairs, reporting directly to the Communications Director.
$48,410.21 - $53,560 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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In Collaboration With The Assistant Dean Of Student Affairs, Provides Advance Level Program Support Directly Related To The Planning And Implementation Of COM Student Activities Including. Under the direction of the Associate Deans for Student Affairs, the Administrative Coordinator manages the administrative functions of the College of Medicine Group on Student Affairs; facilitates and coordinates the efforts of the Associate Dean for Student Affairs, the Associate Deans for Student Career Planning, and the team in the Group on Student Affairs.
$45,530 - $84,241 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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15+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC development of NCEs/small molecules.
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Under the supervision of the Regulatory Program Manager (RPM) of the Regulatory Affairs Unit, the Regulatory Affairs Coordinator (RAC) supports the clinical research efforts of the Chao Family Comprehensive Cancer Center by providing comprehensive, regulatory management of cancer-related protocols in accordance with human subject federal regulations, internal standard operating procedures (SOPs), and University policies and procedures.
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BryceTech is looking for an experienced Regulatory Affairs Analyst to support the DHS FEMA, Office of Response and Recovery, CBRN program, supporting the Office of Emerging Threats Professional and Technical Services Contract.
$95,000 - $105,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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DEFTEC Corporation is seeking a Legislative Affairs Specialist who will support the drafting, editing, and review of DARPA responses to congressional requests for information, briefings, and hearings.
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CMC Regulatory Affairs, oncology, small molecule, drug development, clinical development. Director, CMC Regulatory Affairs. Serve as the PDM regulatory representative on project teams, provide CMC regulatory support for the clinical development of the investigational product(s), and ensure applicable regulatory requirements are appropriately met.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Scientific Affairs & Regulatory Affairs. The Sr. Scientist II will u execute the scientific affairs strategy for your respective categories and geographical area using your scientific and regulatory expertise.
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I have a talented group of recruiters who specifically source Technical Sales Professionals, Scientists, Regulatory Affairs, Scientific Affairs, Executive Technical professionals, Quality Assurance, Product Development, Technical Service, Nutrition, Analytical and Corporate Chefs.
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In collaboration with the Clinical Affairs Lead and Medical/Scientific Lead, prepares strategy decisions, presents, and discusses data at relevant team, governance, external consultants, KOL and potentially regulatory meetings.
$145,400 - $269,400 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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A scientific degree with directly relevant professional experience in global CMC regulatory affairs and CMC technical areas of at least 20 years with a BA/BS, MA/MS, PhD or PharmD. Lead the execution of global CMC regulatory plans, including overseeing the submission and approval process in close partnership with other functions in Research and Development, Regulatory Affairs, and Clinical Development.
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The Regulatory Affairs Specialist supports the oversight of regulatory matters and strategy implementation to ensure the organization complies with applicable regulations. Regulatory Affairs Specialist.
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The Associate, Regulatory Affairs will be a critical team member supporting regulatory strategy and submissions for the firm’s Neuro, Digital Health, and AI/Imaging clientele. 1-3 years of experience in regulatory affairs related to medical devices, drugs and/or biologics, assisting in the writing and/or reviewing of regulatory submissions.
$50,000 - $70,000 a yearFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Represents Clinical Affairs line in program-wide functions on Clinical Project Team, Medical Sub Committee, Clinical Study Teams, Asset Team, Program Teams, and Regulatory Strategy teams as applicable.
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affairs job Title: regulatory specialist Company: Parexel
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