• Merck & Co. (Boston, MA)
    …Atherosclerosis & Metabolism medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the entire ... execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director May Be Responsible For: Evaluating pre- clinical and… more
    HireLifeScience (06/07/25)
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  • Merck & Co. (Boston, MA)
    …and will interact externally with key opinion leaders.-Specifically, the Executive Director may be responsible for:Evaluating pre- clinical and translational work ... opportunities.Managing other Directors and/or Senior Directors responsible for Atherosclerosis clinical development projectsThe Executive Director may supervise… more
    HireLifeScience (06/07/25)
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  • Eisai, Inc (Nutley, NJ)
    …If this is your profile, we want to hear from you. The Associate Director , Clinical Programming must have expertise in addressing technical challenges in the ... be responsible for implementing new technological solutions for end users.The Associate Director , Clinical Programming manages and oversees JReview and SAS… more
    HireLifeScience (06/06/25)
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  • Eisai, Inc (Nutley, NJ)
    …and make a difference. If this is your profile, we want to hear from you. Director , Clinical Quality Assurance The Director , Clinical Quality Assurance ... office. Eisai Salary Transparency Language:The base salary range for the Director , Clinical Quality Assurance is from :195,000-256,000Under current guidelines,… more
    HireLifeScience (06/06/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …managing multiple direct reports. Responsibilities:Operational Strategy:Align with the Head of Clinical Development Operations or Senior Director , Clinical ... areas centered around rare diseases and immune disorders. Job Summary: Senior clinical operational leader accountable for operational planning and execution of FIH,… more
    HireLifeScience (03/28/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full ... company Research Laboratories portfolio of clinical trials.- GCS is accountable for the planning, sourcing, labeling, packaging and delivery of clinical supplies… more
    HireLifeScience (05/29/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …authoring, and management of Dose Preparation Instructions in support of clinical studies being conducted globally by Daiichi Sankyo. The candidate will ... collaborate globally with Formulation and Analytical Scientists, Clinical Operations, Regulatory Affairs CMC, and Clinical Development to collate the necessary… more
    HireLifeScience (05/18/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. ... documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to Clinical more
    HireLifeScience (05/13/25)
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  • Merck & Co. (New York, NY)
    …Adaptability, Biopharmaceutics, Clinical Development, Clinical Oncology, Clinical Testing, Cross-Cultural Awareness, Customer Education , Diversity and ... are seeking a Growth and Improvement minded Oncology Regional Medical Scientific Director that can help drive our Strategic Operating Priorities. Invent-- Pursue the… more
    HireLifeScience (06/03/25)
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  • Merck & Co. (North Wales, PA)
    Job DescriptionRole SummaryThe Regional Medical Scientific Director is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in ... questions about Company products. The work of an Regional Medical Scientific Director is aligned to: Scientific Exchange, Research, Scientific Congress Support, and… more
    HireLifeScience (06/12/25)
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