• Genmab (NJ)
    …(eg competitive landscape) that represent operational risks for the execution of clinical trials within the given indication/program.Key contributor to the ... of all aspects of clinical drug development, with particular emphasis on clinical trial design, trial execution, and strong knowledge about the… more
    HireLifeScience (05/16/25)
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  • Genmab (NJ)
    …Genmab SDTM and ADaM database standards. Supports specification and pooling of data across clinical trials within the same project . Supports submissions by ... other functions including Data Management, Statistics, Drug Safety, Medical, Clinical Pharmacology,Translational Research, Medical Writing, Project management,… more
    HireLifeScience (04/05/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Collaboration and partnership with other functions and stakeholders in supporting clinical trial monitoring and execution through RBQM activities. Accountable ... technical and career, of direct reports, and mentors or acts as functional manager of skip-level or ex-US staff. This position requires strong knowledge about RBQM,… more
    HireLifeScience (05/27/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …and leads technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing ... manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub team and the RA team and serves… more
    HireLifeScience (05/15/25)
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  • Sr. Specialist, Clinical Supplies…

    Merck (Rahway, NJ)
    …Inventory Management Section of the GCS Planning organization. Working independently, the Inventory Manager Clinical Supplies Project Manager (IM CSPM) ... chain across the full company Research Laboratories portfolio of clinical trials . GCS is accountable for the...but are not limited to:** + Participates on the Clinical Trial Team (CTT) and collaborates closely… more
    Merck (05/30/25)
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  • Sr. Specialist, Clinical Supply…

    Merck (Rahway, NJ)
    …and the operational/executional arms within the business. Working independently, the Protocol Clinical Supplies Project Manager (Protocol CSPM) designs ... chain across the full company Research Laboratories portfolio of clinical trials . GCS is accountable for the...spokesperson at clinical development related meetings (ie, Clinical Trial Teams) and product development related… more
    Merck (05/30/25)
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  • Associate Director, Clinical Supply…

    Merck (Rahway, NJ)
    … development teams and the operational/executional arms within the business. The Program Clinical Supplies Project Manager (Program CSPM) serves as the ... chain across the full company Research Laboratories portfolio of clinical trials . GCS is accountable for the... Management Skills: strong knowledge of the principles of project management and clinical customer relationship management.… more
    Merck (05/30/25)
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  • Sr. Manager , Clinical Research…

    Taiho Oncology (Princeton, NJ)
    …Performance Objectives: + Collaborates with other key team members (Medical monitor, Project Manager , Clinical Operations, Data Management, Biostatistics, ... Biomarkers and Medical Writing etc.), to deliver high quality clinical trial results. + Use scientific expertise...+ Keeps Sr. Medical Director current on status of clinical trials and provides ongoing risk assessments… more
    Taiho Oncology (04/08/25)
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  • Associate Clinical Project

    IQVIA (Parsippany, NJ)
    …required, Nursing experience in addition to this is ideal!_ **Job Overview** Associate Clinical Project Managers (aCPM)/Local Trial Managers are an integral ... contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on ...combined with experience * Knowledge of clinical trials - Knowledge of clinical trial more
    IQVIA (06/06/25)
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  • Senior Financial Analyst, Clinical

    Vitalief (New Brunswick, NJ)
    …senior leadership of clinical trial revenue activity including active clinical trials and research subjects. Required Skills: + Bachelor's Degree in ... working at the intersection of Sites, Sponsors, and CROs across the research and clinical trials landscape. By blending deep subject matter expertise with strong… more
    Vitalief (04/07/25)
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