• Regulatory CMC Project

    Parexel (Raleigh, NC)
    …innovative treatment options to patients. We are currently seeking a dedicated and detail-oriented ** Regulatory CMC Project Manager ** to join a growing, ... requirements. Project Management: Serve as the project manager for meetings, adhering to best...Project Management). + 3+ years proven experience in regulatory affairs, particularly in CMC (Chemistry, Manufacturing,… more
    Parexel (12/12/25)
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  • Senior Manager , CMC Global…

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    …of regulatory guidelines and perspective to the cross-functional team. Serve as CMC regulatory lead on global project teams (Pharmaceutical Development, ... domestic/international travel. **Job Description** + Develop and implement global CMC regulatory strategies for late-stage development, marketing applications… more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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  • Senior Specialist, Digital CMC

    Merck (Raleigh, NC)
    …Informatica Metadata Manager , Management Process, Process Flow Documentation, Project Management, Regulatory Documents, SAP Master Data Governance (MDG), ... development through commercialization, with practical insight into how these operations generate CMC regulatory content + Understanding of CMC operations,… more
    Merck (12/02/25)
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  • Senior Manager , Global Regulatory

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    …of the associated regulatory challenges to the GRL, global regulatory team, assigned project teams, and internal/external functional business units ... associated regulatory challenges to the GRL, global regulatory team, assigned project teams, and internal/external...needed. - Works collaboratively with members of the global regulatory team (GRL, regional leads, CMC -RA, labeling,… more
    Otsuka America Pharmaceutical Inc. (11/20/25)
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  • Sr Director, Project Management,…

    ThermoFisher Scientific (Greenville, NC)
    …+ Capable of working independently and exercising independent judgment to assess sponsor regulatory needs and work with project team members to producing ... of ICH and other global regulatory guidelines; in-depth understanding of a regulatory specialty areas, such as preclinical, clinical, CMC , publishing, etc. +… more
    ThermoFisher Scientific (12/03/25)
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  • Sr Oversight Director, Project Management…

    ThermoFisher Scientific (Greenville, NC)
    …+ Capable of working independently and exercising independent judgment to assess sponsor regulatory needs and work with project team members to producing ... depend on - now and in the future. Our Project Delivery colleagues within our PPD(R) clinical research services...global regulatory guidelines; in-depth understanding of a regulatory specialty areas, such as preclinical, clinical, CMC more
    ThermoFisher Scientific (10/15/25)
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  • Senior Clinical Trial Manager , FSP

    ThermoFisher Scientific (Wilmington, NC)
    …consent templates and other protocol specific documents as required. Collaborates with the project manager to prepare, organize, and present at client meetings, ... members involved in the study set up (DM, Reg, CMC etc ): ensure feasibility report are exhaustive, Review...activity timelines and metrics, providing status updates to the project manager , regularly reviewing projects using tracking… more
    ThermoFisher Scientific (10/25/25)
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  • Senior Manager , Global Product Quality…

    Otsuka America Pharmaceutical Inc. (Raleigh, NC)
    regulatory submissions for OPDC R&D products. Performs quality reviews of CMC sections of regulatory submissions. + Authors and maintains Standard Operating ... The Senior Manager , Global Product Quality - Biologics is responsible...Subsidiaries ensure Compliance with local and global requirements and regulatory requirements. + Interfaces with project teams… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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