• Quality Event Investigator

    Catalent Pharma Solutions (Greenville, NC)
    …is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for ... turn-key solutions for oral solid dosage forms, including integrated formulation development , analytical services, commercial manufacturing, and packaging . This… more
    Catalent Pharma Solutions (01/05/24)
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  • Senior Lead Investigator , Technical…

    Catalent Pharma Solutions (St. Petersburg, FL)
    **Position Summary** St. Petersburg is our primary softgel development and manufacturing facility in North America with a capacity of 18 billion capsules per year. ... product introduction process. The primary tasks performed by the **Senior Lead Investigator ** will include working on proper investigation and documentation of the… more
    Catalent Pharma Solutions (02/29/24)
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  • Operations Manager - Device Assembly…

    Lilly (Concord, NC)
    …with or understanding of:** + Working within or directly supporting pharmaceutical , food, packaging , or applicable manufacturing departments + Highly ... will house warehousing & logistics, parenteral operations, medical device assembly, and packaging , QC laboratories, and support teams to produce medicines for an… more
    Lilly (01/17/24)
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  • Kelly/NIH Clinical Advisor (Licensed Pharmacist)

    Kelly Services (Rockville, MD)
    …protocol development meetings, and protocol team meetings as a pharmaceutical subject matter expert. * Attend and participate in US/Non-U.S scientific ... shall provide services in support of the overall functions of the Pharmaceutical Affairs Branch, Office of Clinical Site Oversight, DAIDS **_._** **_Technical… more
    Kelly Services (03/01/24)
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  • Manager, Clinical Trials

    Grifols Shared Services North America, Inc (Research Triangle Park, NC)
    …Responsibilities:** + Manages direct reports including performance evaluations and professional development . + Oversees third party vendors as well as develops and ... required clinical documents for submission to regulatory authorities (eg, protocols, investigator brochures, clinical study reports), as necessary. + Manages overall… more
    Grifols Shared Services North America, Inc (03/26/24)
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  • Associate Director, Clinical Operations

    Grifols Shared Services North America, Inc (Research Triangle Park, NC)
    …**Primary responsibilities for role:** + Develops and manages clinical development program plans (eg, strategies, budgets, timelines). + Provides clinical ... clinical data prior to submission to regulatory authorities (eg, protocols, investigator brochures, clinical study reports). + Manages clinical timelines, budgets,… more
    Grifols Shared Services North America, Inc (03/01/24)
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  • Business Continuity Project Management Global…

    Merck (West Point, PA)
    …and project team meetings to provide a broad perspective on the drug development process in the pharmaceutical industry. Required Education and Experience: + ... trials run in-house, 400+ outsourced or run by partners, and 300+ company Investigator Initiated Studies (IIS) clinical trials. GCS is accountable for the planning,… more
    Merck (03/14/24)
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