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Regulatory Submissions Manager jobs

Viewing 31 - 40 of 18,247 jobs

  • Regulatory Submissions Specialist - Documentum/ eCTD

    Tech Observer - Elizabeth, NJ

    e-documentation support activities as necessary Provide regulatory support to Reg CMC managers, collection of ... appropriate candidate, submission planning and strategic regulatory preparation activitiesAdministrative Tasks:...

    14 days ago from Get Clinical Research Jobs

  • Director - Regulatory Affairs - OPDP Liaison

    Diedre Moire - North Carolina

    experience in pharmaceutical industry interfacing with regulatory representatives from the FDA OPDP. Join a well ... Advertising Lead Marketing Specialist Pharma Advertising Regulatory Affairs Representative Label Promotion Review...

    10 days ago from Diedre Moire

  • Manager/Sr. Manager, Regulatory Affairs

    Dermira - Menlo Park, CA

    for regulatory submissions. • Communicate timelines for regulatory submissions to affected individuals and departments, ... with regulatory team at CROs to ensure timely submissions to ex-US regulatory agencies when applicable. • Serve as...

    26 days ago from Biospace

  • Project Management Office Professional

    Compliance Search Group - New York City, NY

    • Experience in regulatory delivery or regulatory PMO • Compliance and Regulatory delivery experience • Experience ... approvals, submissions, sign-offs etc. Pre-emptively communicate status to appropriate parties • Ownership and...

    15 hours ago from The Ladders

  • GMP Quality Manager

    Takeda Pharmaceuticals - Cambridge, MA

    States OBJECTIVE The GMP Quality Manager leads and manages strategic GMP QA activities ... packagers,and laboratories) related to Takeda regulatory submissions. Effectively interact with QA senior...

    30+ days ago from Takeda Pharmaceuticals

  • Senior Submission Writer

    Novartis Oncology - East Hanover, NJ

    production of high quality clinical documentation for HA submissions. Provides authoritative documentation related ... Experience of coordinating writing activities for regulatory submissions. • Submission expertise evidenced by...

    30+ days ago from Biospace

  • Clinical Project Manager

    Scientific Search - Oakland, NJ

    Prepare the study budget in consultation with project management/line manager/business development for the assigned proj ... Assist in preparation of dossier and/or appropriate documentation for regulatory/ethics committee submission or other ap...

    21 days ago from The Ladders

  • QA Regulatory Affairs Specialist

    Online Technical Services - San Diego, CA

    for ensuring that products and their labeling meet all regulatory requirements (national and international). ... FDA QSRs (GMP) (including company registration, new product submissions, establishing FDA communicationchannels for...

    27 days ago from Dice

  • Director, Research

    HCA Healthcare - Aventura, FL

    approved research projects. • Provide regulatory, ethical, and methodological advice to individual principal ... CERTIFICATE/LICENSE • Certified IRB Professional (CIP) or Certified IRB Manager (CIM) credential or eligibility and comm...

    16 days ago from HCA Healthcare

  • Global Program Regulatory Affairs Manager / Associate Director

    Novartis Oncology - Cambridge, MA

    The Global Program Regulatory Affairs Manager / Associate Director provides regulatory leadership for early projects in ... • 2-4 years (Manager), 3-5 years (Associate Director) of regulatory experience with a strong knowledge of US...

    30+ days ago from Biospace