• Senior Professional Services Veterinarian-…

    Merck (Indianapolis, IN)
    **Job Description** The Senior Professional Services Veterinarian- Dermatology Specialist will function to support the commercial, medical, and business needs of the ... may include, but are not limited to: + Utilizes specialist knowledge and experience in dermatology to serve as...leaders of diverse expertise and backgrounds, and assist medical affairs in developing and guiding advisory boards + Represent… more
    Merck (04/17/24)
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  • Clinical Safety Specialist

    J&J Family of Companies (Indianapolis, IN)
    …UADEs) per study and regulatory requirements including collaboration with regulatory affairs and clinical operations, or overseeing activities of third-party ... Clinical Safety Specialist - 2406185254W **Description** Abiomed, part of Johnson...DSMB/DMC preferred * Experience with complaint handling, quality & regulatory processes preferred * Strong interpersonal skills and well-developed… more
    J&J Family of Companies (05/03/24)
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  • Community Escalations Specialist , Risk…

    Meta (Indianapolis, IN)
    …to Job" online on this web page. **Required Skills:** Community Escalations Specialist , Risk and Response Responsibilities: 1. Interpret and enforce company terms of ... the most sensitive and complex escalations of public interest involving regulatory and legal requests to resolution, and communicate to cross-functional partners.… more
    Meta (04/23/24)
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  • Associate Vice President-Clinical Design…

    Lilly (Indianapolis, IN)
    …additional items including but not limited to protocols, publications, regulatory interactions, internal executive and governance presentations, external key opinion ... Understand how design elements influence the ability to deliver on new regulatory expectations (eg decentralization of clinical trials, increase racial and ethnic… more
    Lilly (02/29/24)
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  • Clinical Research Scientist, GPS Medical

    Lilly (Indianapolis, IN)
    …in areas relevant to drug discovery or development, eg epidemiology, toxicology, pharmacovigilance, regulatory affairs . OR + 3-5 years of clinical experience, or ... other aggregate reviews of spontaneous or clinical trial data submitted to regulatory agencies and provide analyses and summaries for these reports.Provide Global… more
    Lilly (04/11/24)
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  • Associate Director - Device Safety Scientist…

    Lilly (Indianapolis, IN)
    …areas relevant to drug discovery or development, eg epidemiology, toxicology, pharmacovigilance, regulatory affairs + Experience within Global Patient Safety or ... detection and clarification, preparation of device safety reviews, support for regulatory inquiries, input into device development and risk management activities,… more
    Lilly (04/17/24)
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  • Center Medical Director (CMD)

    CSL Plasma (Indianapolis, IN)
    …Staff Associates for completion of training and recommendation for certification by Regulatory Affairs . Functionally directs the Center Medical Staff. Provides ... related topics. Documents each meeting. Meets with the Center Manager and Compliance Specialist (or designees) during weekly visits to the center. Serves as a member… more
    CSL Plasma (04/16/24)
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