Results, order, filter

Regulatory Affairs Manager Jobs in New York

  • Manager, Regulatory Affairs CMC

    Regeneron Pharmaceuticals - Troy, New York
    ... Keeps management and all partners up to date of assessments, overall strategy, and project status ... :** Contributes to the management of the regulatory submission form process, which involves the review of ...
  • Manager, Regulatory Affairs CMC

    Regeneron Pharmaceuticals - Sleepy Hollow, New York
    ... Keeps management and all partners up to date of assessments, overall strategy, and project status ... :** Contributes to the management of the regulatory submission form process, which involves the review of ...
  • Manager, Regulatory Affairs CMC

    Regeneron Pharmaceuticals - Rensselaer, New York
    ... Keeps management and all partners up to date of assessments, overall strategy, and project status ... :** Contributes to the management of the regulatory submission form process, which involves the review of ...
  • Manager, Regulatory Affairs CMC

    Regeneron Pharmaceuticals - Armonk, New York
    ... Keeps management and all partners up to date of assessments, overall strategy, and project status ... :** Contributes to the management of the regulatory submission form process, which involves the review of ...
  • Regulatory Affairs Manager

    ICON Clinical Research - Farmingdale, New York
    ... , able to effectively manage matrix teams and have regulatory project management experience. The ... includes Regulatory Project Management experience for timely and accurate completion of assigned projects ...
  • Senior Manager, Regulatory Affairs - General Medicine

    Regeneron Pharmaceuticals - Tarrytown, New York
    ... following:** Coordinate the preparation, submission, management and maintenance of global ... interacting with CROs in the management of ex-US/ex-EU CTAs towards clinical trial activations preferred ...
  • Manager, Regulatory Affairs - Solid Oncology

    Regeneron Pharmaceuticals - Tarrytown, New York
    ... :** Coordinate the preparation, submission, management and maintenance of global regulatory submissions related ... interacting with CROs in the management of ex-US/ex-EU CTAs towards clinical trial activations preferred ...