• Merck & Co. (Rahway, NJ)
    Job DescriptionThe Executive Clinical Director (Distinguished Principal Scientist) has primary responsibility for the strategic planning and directing ... compounds in Immunology. With a focus on late-stage development, the Executive Clinical Director will manage the entire cycle of clinical development,… more
    HireLifeScience (01/08/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …trial master file is complete and accurate for assigned stud(ies).If assigned, Associate Director , Clinical Operations may act as the Study Team Leader for ... disorders. Job Summary: The incumbent will be responsible for ensuring execution of clinical studies across geographic regions, in adherence to Good Clinical more
    HireLifeScience (01/07/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …around rare diseases and immune disorders. Summary This position works with the Director , Clinical Study Startup to establish the strategy driving global ... make decisions where appropriate and escalate any complex problems to the Director , Clinical Study Startup.This position requires strong organization and… more
    HireLifeScience (01/06/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    Director , Clinical Development Join a Legacy of Innovation 125 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of innovative ... primary source of medical accountability and oversight for one or more clinical trials Matrix management responsibilities across the internal and external network… more
    HireLifeScience (12/20/24)
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  • Merck & Co. (Rahway, NJ)
    …a particular focus on obesity and obesity-related metabolic disorders. - The Senior Director will manage the entire cycle of clinical development, including ... monitoring, analysis, regulatory reporting, and publication. - Specifically, the Senior Director may be responsible for Evaluating pre- clinical and translational… more
    HireLifeScience (01/11/25)
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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 (01/06/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Global Regulatory Affairs and Clinical Safety Global Process Lead is responsible for overseeing and managing Global Regulatory Affairs & ... Clinical Safety global business processes. This includes defining and...management for global processes across Global Regulatory Affairs and Clinical Safety . The Global Process Lead actively engages… more
    HireLifeScience (01/10/25)
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  • Merck & Co. (Rahway, NJ)
    …Our company's Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of ... placement, monitoring, analysis, regulatory reporting, and publication.Specifically, The Senior Director May Be Responsible ForEvaluating pre- clinical and… more
    HireLifeScience (01/11/25)
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  • Merck & Co. (Rahway, NJ)
    …Our company's oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of ... design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, the Director may be responsible for:-Evaluating pre- clinical and… more
    HireLifeScience (01/11/25)
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  • Merck & Co. (Rahway, NJ)
    …approach, driving the development of in vitro-in vivo relationships and preclinical-to- clinical translation in bioperformance of formulationsThe Director will ... oral and non-oral portfolio. Within Biologics and Biopharmaceutics, the Biopharmaceutics Director will influence the strategy, lead activities, and develop a team… more
    HireLifeScience (01/03/25)
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  • Merck & Co. (Rahway, NJ)
    …help people with cancer across the globe.Working with ADT's, early- & late-stage clinical development teams, the BMx leads will develop asset-specific clinical ... biomarker strategy by incorporating critical insight from discovery biology, clinical development, diagnostics, bioinformatics, molecular assay experts, QP2 and… more
    HireLifeScience (12/20/24)
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  • Merck & Co. (Rahway, NJ)
    …network to enable process and formulation development.- In this position the SMAR&D Director will set guidance, lead activities, and develop a team whose roles ... include development of characterization methods to characterize and release clinical drug substance and product and their stability tests, raw materials/excipients,… more
    HireLifeScience (01/11/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Executive Director , Value & Implementation (V&I), Global Medical and Scientific Affairs (GMSA) is accountable for the development and execution of ... TA dedicated global and regional directors and associate directors. The Executive Director , Value & Implementation (referred to as EDMA) engages with global… more
    HireLifeScience (01/11/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionR5 - Director - Pharmacometrics, Quantitative Pharmacology and PharmacometricsT he (remote) position is only applicable for those that are not within ... decision-making at our company, this position offers an opportunity for the Director to drive pipeline impact and mentor/coach a talented group of… more
    HireLifeScience (01/11/25)
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  • Merck & Co. (Rahway, NJ)
    …collaboration to further differentiate our portfolio.The Oncology Regional Medical Scientific Director , RMSD, is a credentialed (ie, MD, PhD, or PharmD) therapeutic ... have a medical contact within the company.Upon request from Global Clinical Trial Operations (GCTO), support Company-Sponsored Trials to enhance the understanding… more
    HireLifeScience (01/10/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …areas centered around rare diseases and immune disorders. Summary The Associate Director of Regulatory Writing is a key role responsible for producing scientifically ... accurate, high-quality clinical regulatory documents while adhering to regulatory guidelines. This...strategic insights at the study team level. The Associate Director of Regulatory Writing must possess advanced knowledge of… more
    HireLifeScience (01/08/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …initiative in support of these objectives. This position will report to the Sr Director , Group Leader, GPM&L or the Executive Director , US Head GPM&L. ... execution of the integrated product development plan.Partners with the Clinical Team Leader to ensure a high performing ...Clinical Team Leader to ensure a high performing Clinical Sub-team and to drive the development and delivery… more
    HireLifeScience (01/10/25)
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  • Merck & Co. (Rahway, NJ)
    Job Description Overview: The Director , Global Media Relations, is responsible for developing and executing a global media strategy that showcases our Company's ... development, product approvals, thought leadership, policy, and overall performance. The director will build and maintain strong working relationships with pharma,… more
    HireLifeScience (01/07/25)
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  • Merck & Co. (Rahway, NJ)
    …trials and will interact externally with key opinion leaders.-Specifically, the Executive Director , PDT lead may be responsible for:-Evaluating pre- clinical and ... of external opportunities.-Provide support for other therapeutic areas regarding clinical issues related to oncology compounds.-The Executive Director /PDT… more
    HireLifeScience (01/11/25)
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  • Merck & Co. (Rahway, NJ)
    …Reporting to the AVP Global Market Access, Global Pharma, the Executive Director , Global Market Access, Infectious Disease & Ophthalmology will be a member ... team and will lead a team across the ID&O portfolio.T he Executive Director , Global Market Access, Infectious Disease & Ophthalmology will play a leadership role… more
    HireLifeScience (01/06/25)
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