• Sr. Medical Director, Clinical Development (GU…

    Bristol Myers Squibb (Princeton, NJ)
    …to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial and regulatory documents + Conduct investigator ... and nonclinical studies into clinical development opportunities + Oversee Data Review and Independent Data Monitoring Committees + Conduct clinical trials using… more
    Bristol Myers Squibb (07/08/25)
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  • Legal Program Director

    State of Connecticut, Department of Administrative Services (Hartford, CT)
    …as an attorney with some responsibility for research, development, planning and review of legislative and/or regulatory and/or legal programs? The State of ... a team of attorneys and paralegals focused on the regulation of the pharmaceutical , cannabis and hemp industries + Assist with developing and operationalizing policy… more
    State of Connecticut, Department of Administrative Services (09/26/25)
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  • Senior QA/RA Specialist

    Charles River Laboratories (Northridge, CA)
    …the highest quality cellular material and services to biotech and pharmaceutical companies and research organizations that are performing innovative research and ... oversee the management of regulatory documentation related to the organization's Institutional Review Board (IRB) activities. Will assist with the new and ongoing… more
    Charles River Laboratories (09/24/25)
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  • Manager, Regulatory Affairs - Advertising…

    Regeneron Pharmaceuticals (Sleepy Hollow, NY)
    …to conference exhibit activities, disease awareness and speaker programs + Provide review of US and Global (if applicable) product and disease state ... company policies. + Ability to identify process improvement for promotional review activities that would enable the establishment of portfolio wide standardization… more
    Regeneron Pharmaceuticals (09/06/25)
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  • Senior Manager, Regulatory Affairs Advertising…

    Regeneron Pharmaceuticals (Sleepy Hollow, NY)
    …to conference exhibit activities, disease awareness and speaker programs + Provide review of US and Global (if applicable) product and disease state ... input to direct management with respect to process improvement for promotional review activities and establishment of portfolio wide standardization of policies +… more
    Regeneron Pharmaceuticals (07/03/25)
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  • Vice President, Regulatory Affairs - Oncology

    Sumitomo Pharma (Harrisburg, PA)
    Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... + Oversee the regulatory activities at CROs, providing document review in order to ensure the quality and scientific...by law. Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in… more
    Sumitomo Pharma (09/23/25)
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  • Microbiologist II

    The Ritedose Corporation (Columbia, SC)
    …in-process product testing. Other responsibilities include data entry, data review , ensuring calibration of equipment, maintaining inventory of laboratory supplies, ... VITEK MS - Raw Material Testing including APIs - Review - Growth Promotion Level 2 - Minimum 2...Growth Promotion Level 2 - Minimum 2 years of Pharmaceutical EM and Microbiology laboratory - Endotoxin Testing -… more
    The Ritedose Corporation (09/23/25)
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  • Conventions Manager

    Bausch + Lomb (Bridgewater, NJ)
    …meetings and lead management. Administrative functions included such as contract review , purchase orders and invoicing. + Create and obtain Medical, Legal ... of convention content and final exhibit plans/renderings through our Promotional Review Committee (PRC). + Responsible to produce, track and maintain current,… more
    Bausch + Lomb (09/10/25)
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  • Quality Assurance Specialist IV - Therapeutics

    LGC Group (Petaluma, CA)
    …and inspection readiness within organization. + Investigations: Performance and review for investigations associated with Complaints, Deviations, CAPA, OOS, Out ... Atypical Results, Environmental Discrepancy Reports and Alert Level Reports. + Batch Review : Perform technical review of the manufacturing batch records and… more
    LGC Group (09/07/25)
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  • Associate Director, Corporate Counsel

    Amneal Pharmaceuticals (Bridgewater, NJ)
    …The incumbent will serve as a member of Amneal's promotional assets review committee (PARC), draft/ review /negotiate general commercial and other types of ... Advise on a broad array of issues relating to the marketing and promotion of pharmaceutical products and actively represent Legal on the company PARC to review more
    Amneal Pharmaceuticals (07/30/25)
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