• Merck & Co. (Rahway, NJ)
    Job DescriptionPosition Description: Senior Specialist , Clinical Literature MonitoringProvides pertinent and timely information on our Company's products and ... search request results meet current regulatory requirements Collaborates with pharmacovigilance teams to meet current literature-related adverse event monitoring… more
    HireLifeScience (03/22/24)
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  • Merck & Co. (North Wales, PA)
    …partners with functional leaders and teams within Digital Clinical Measures (DCM), Global Clinical Operations team (GCTO) and Business Development (BD) to assess the ... requirements. In the clinical arena, RDH works with key functional groups within Global Regulatory Affairs, GCTO and others to implement the regulatory strategy for… more
    HireLifeScience (02/28/24)
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  • 安全管理(ファーマコビジランス)業務従事者/ Senior

    Mallinckrodt Pharmaceuticals (Jobe, MO)
    Job Title 安全管理(ファーマコビジランス)業務従事者/ Senior Specialist , Pharmacovigilance Requisition JR000012874 安全管理(ファーマコビジランス)業務従事者/ Senior Specialist , ... Locations Kobe Job Description 医療用医薬品の安全管理業務を中心に担っていたいだくポジションです。担当いただく製品は国内外で販売されており、当該医薬品の個別症例情報・文献情報の取扱いとそれらに関連する業務を中心に担っていただきます。業務にあたっては Global PVチーム及び国内提携会社との連携も必要となります。 チーム全体で以下の業務を担っています。中心業務の他については、これまでのご経験に合わせて分担して対応いただきます。 GVPに基づく安全性情報の処理… more
    Mallinckrodt Pharmaceuticals (02/09/24)
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  • CRP Safety and Pharmacovigilance Manager…

    University of Pennsylvania (Philadelphia, PA)
    … Manager (Center for Cellular Immunotherapy) Job Profile Title Clinical Research Monitoring Specialist Senior Job Description Summary The CRP Safety and ... design related to clinical safety management + Extensive knowledge of FDA / global clinical trial regulations and ICH GCP Guidelines + Understanding of the clinical… more
    University of Pennsylvania (01/19/24)
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  • Senior Specialist , Clinical…

    Merck (North Wales, PA)
    **Job Description** **Position Description:** Senior Specialist , Clinical Literature Monitoring Provides pertinent and timely information on our Company's ... request results meet current regulatory requirements + Collaborates with pharmacovigilance teams to meet current literature-related adverse event monitoring… more
    Merck (03/22/24)
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  • Senior Specialist , Clinical Risk…

    J&J Family of Companies (Horsham, PA)
    Senior Specialist , Clinical Risk Management - Neuroscience - 2406176854W **Description** Janssen Research & Development, LLC, a member of the Johnson & Johnson ... family of companies, is recruiting for a ** Senior Specialist , Clinical Risk Management - Neuroscience**...diverse styles and business approaches by understanding regional and global business structures is required + Knowledge of Good… more
    J&J Family of Companies (03/26/24)
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  • Medical Director or Senior Scientific…

    AbbVie (Mettawa, IL)
    …on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description Provides specialist medical/scientific strategic and operational leadership into global ... all applicable laws and regulations. Responsibilities: + Leads a team of 3-4 global pipeline scientific/ medical directors. + Leads and partners on the development… more
    AbbVie (03/18/24)
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  • Sr Specialist , Regulatory Digital Health…

    Merck (North Wales, PA)
    …partners with functional leaders and teams within Digital Clinical Measures (DCM), Global Clinical Operations team (GCTO) and Business Development (BD) to assess the ... clinical arena, RDH works with key functional groups within Global Regulatory Affairs, GCTO and others to implement the...networking opportunities within and beyond RDH . Exposure to Senior level positions within the metrics process . Hands-on… more
    Merck (02/28/24)
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  • Associate Director - Device Safety Scientist…

    Lilly (Indianapolis, IN)
    …in areas relevant to drug discovery or development, eg epidemiology, toxicology, pharmacovigilance , regulatory affairs + Experience within Global Patient Safety ... to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work… more
    Lilly (02/28/24)
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  • Director/ Senior Associate Director,…

    Boehringer Ingelheim (Ridgefield, CT)
    **Description** The role of Senior Clinical Program Leader (CPL) - Retinal health, assumes full medico-scientific and strategic leadership of clinical programs with ... accelerate clinical development and achieve regulatory approvals and reimbursable medicines. Senior CPL provides continuous medical benefit and risk oversight for… more
    Boehringer Ingelheim (02/27/24)
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  • ( Senior Associate Director/Director)…

    Boehringer Ingelheim (Ridgefield, CT)
    …+ Strong project management skills. + Agile and effective working style. ** Senior Clinical Program Leader Requirements:** + MD ( specialist in respective ... and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering… more
    Boehringer Ingelheim (02/01/24)
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  • Late-Stage Clinical Development Leader

    Organon & Co. (Plymouth Meeting, PA)
    …and is accountable for: + The leadership of the following teams: Global Clinical Development (GCD), Clinical Trial Operations (CTO), Clinical Data Sciences (CDS) ... issues and risks. + As member of the Organon Senior Leaders team contributing by driving our Company into...from other areas. + Leadership of the following teams: Global Clinical Development, Clinical Trial Operations, Clinical Data Sciences,… more
    Organon & Co. (03/12/24)
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  • Director, External Scientific Collaborations (US…

    AbbVie (IL)
    …innovative and strategic projects and priorities for USMA oncology. Provides specialist medical/scientific strategic and operational input into core medical affairs ... during engagements + Strong, proven relationship management skills with senior leaders (eg C-suite leaders, industry-affairs office personnel, thought leaders,… more
    AbbVie (03/29/24)
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