• Director Regulatory Affairs

    Teva Pharmaceuticals (West Chester, PA)
    Director Regulatory Affairs - Submission Management - West Chester, PA Date: Apr 20, 2024 Location: West Chester, United States, Pennsylvania, 19380 ... Medicine Dossier Project Manager, a key member of Global Regulatory Affairs , will be responsible to develop...This role requires utilization of in-depth knowledge of global regulatory submission requirements, processes and procedures, eCTD… more
    Teva Pharmaceuticals (03/23/24)
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  • Senior Director , Regulatory

    Teva Pharmaceuticals (West Chester, PA)
    Senior Director , Regulatory Affairs II Date: Apr 20, 2024 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job Id: ... to make a difference with. **The opportunity** The Senior Director , Regulatory Affairs II will...how systems are integrated to support day to day regulatory and submission publishing business processes with… more
    Teva Pharmaceuticals (02/23/24)
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  • Senior Director Regulatory

    Teva Pharmaceuticals (West Chester, PA)
    Senior Director Regulatory Affairs CMC (Biologic Products) Date: May 15, 2024 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva ... to make a difference with. **The opportunity** The Sr. Director , Global Regulatory Affairs CMC...the development teams. ⦁ Develop and communicate effective CMC regulatory strategies for development and post marketing submission more
    Teva Pharmaceuticals (05/16/24)
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  • Director , Regulatory Affairs

    Teva Pharmaceuticals (West Chester, PA)
    Director , Regulatory Affairs , Strategy - Innovative Medicine (West Chester, PA or Remote) Date: Apr 29, 2024 Location: West Chester, United States, ... people to make a difference with. **The opportunity** The Director , Global Regulatory Affairs , is...regulatory knowledge of IND and NDA/BLA content and submission experience. Working within Teva Innovative Medicines, this role… more
    Teva Pharmaceuticals (05/04/24)
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  • Director Clinical Development - Immunology

    Teva Pharmaceuticals (West Chester, PA)
    …as needed + Partners cross-functionally with departments such as Regulatory Affairs , Toxicology, CMC/Formulations, Biostatistics, Legal, Marketing, ... key documents (ie protocols, Investigator's Brochures, clinical study reports, summaries for regulatory submissions). The Director will provide input to the… more
    Teva Pharmaceuticals (03/02/24)
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  • Contract & Grants Analyst - Research Office

    University of Delaware (Newark, DE)
    …process award in UD Grants System, interface with the Associate Vice President, Research and Regulatory Affairs and Director , Regulatory Affairs to ... administrators frequently to resolve issues or interpret policy. Proposal Submission : + Compile and analyze data in the processing...+ Consult with the Associate Vice President, Research and Regulatory Affairs and Director , … more
    University of Delaware (03/28/24)
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