• Genmab (Plainsboro, NJ)
    …best, and authentic is essential to fulfilling our purpose.The RoleThe Global Clinical Trial Manager (GCTM) is accountable for the end-to-end delivery of a single or ... from strategy outline through to CSR by leading cross-functional trial specific Clinical Trial Teams (CTT) to...be innovativeYou have experience working in a fast-growing, dynamic company (or a strong desire to)You work hard and… more
    HireLifeScience (12/04/24)
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  • Merck & Co. (Rahway, NJ)
    …those scientific leaders to ensure they have a medical contact within the company .Upon request from Global Clinical Trial Operations (GCTO), support Company ... balanced, factual, scientific information about non-product areas of interest to the company . The RMSD provides research support to our Investigator-Sponsored and … more
    HireLifeScience (01/10/25)
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  • Genmab (Plainsboro, NJ)
    …Drug Supply Manager, of the following tasks:Global Clinical Drug Supply Project/ Trial ManagementObtain Project/ Trial specific information to initiate drug supply ... may impact clinical drug supply)Create and maintain program/project and trial IMP/AMP forecast and demand plans throughout the ...be innovativeYou have experience working in a fast-growing, dynamic company (or a strong desire to)You work hard and… more
    HireLifeScience (01/07/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …external service providers (CROs, vendors, etc.) and clinical sites to ensure all trial deliverables are met according to timelines, budget, quality standards and in ... compliance. Proactively track, monitor and report trial risks, progress/performance, timelines, and financial metrics on an...10-20% overnight travel required. May be required to work company holidays and weekends. The incumbent can work from… more
    HireLifeScience (01/04/25)
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  • Merck & Co. (North Wales, PA)
    …This may include:Serving as the lead clinical scientist on the clinical trial team.Leading medical monitoring team in review and interpretation of clinical ... clinical data to ensure quality, completeness, and integrity of trial conduct.Providing tactical/scientific mentorship to other clinical scientist.Core Skills Solid… more
    HireLifeScience (01/11/25)
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  • Merck & Co. (Rahway, NJ)
    …and Research Decision Sciences), a distinguished department within our Company 's renowned Research and Development division, quantitative scientists, in partnership ... field plus 9 years SAS/R programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering… more
    HireLifeScience (01/09/25)
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  • Genmab (Plainsboro, NJ)
    …an initiative driven and proactive player with responsibility to deliver high quality trial supplies on time from an planning perspective. Changes are a natural part ... and Operational ExecutionOversee strategic and operational plans for clinical trial drug supply.Maintain agreements, contracts, and SOPs to support efficient… more
    HireLifeScience (01/07/25)
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  • Genmab (Plainsboro, NJ)
    …play a pivotal role in ensuring the timely delivery of high-quality clinical trial supplies for both early and late-stage trials. In addition, this position offers ... a highly competent global team focused on packaging and labeling clinical trial supplies, collaborating closely with the Global Clinical Drug Supply Planning team.… more
    HireLifeScience (12/19/24)
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  • Genmab (Plainsboro, NJ)
    …Responsible for coordinating sourcing for new trials to ensure efficient and effective trial operations.Point of Contact for Global Clinical Trial Managers: Act ... and resolve issues.Vendor Owner:First Point of Contact for clinical trial vendors: Serves as the first point of contact...be innovativeYou have experience working in a fast-growing, dynamic company (or a strong desire to)You work hard and… more
    HireLifeScience (12/04/24)
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  • Merck & Co. (Rahway, NJ)
    …chain across the full of our Research & Development Division portfolio of clinical trial s .- GCS is accountable for the planning, sourcing, labeling, packaging and ... s as the GCS spokesperson at clinical development related meetings (i .e., Clinical Trial Team s ) and product development related meetings . The incumbent must have… more
    HireLifeScience (01/16/25)
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  • Merck & Co. (Rahway, NJ)
    …will join our Project Management Office (PMO) for one of our Company 's Enterprise-wide Accelerate multiyear program, that focuses on technology and process ... platformTransform the way we conduct our clinical trials.Improve the clinical trial experience for our patients.Improve efficiency, reduce cycle time and enable… more
    HireLifeScience (01/15/25)
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  • Merck & Co. (North Wales, PA)
    …and Research Decision Sciences), a distinguished department within our company 's renowned Research and Development division, quantitative scientists, in partnership ... and at least 5 years SAS programming experience in a clinical trial environment orMS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering… more
    HireLifeScience (01/08/25)
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  • Aequor (South San Francisco, CA)
    …is to optimize the support of clinical systems to provide high-quality clinical trial data insights and to offer data science-related consultation to the study ... for the ECD specific RBQM analysis solutions. Champion RBQM within the company and collaborate with cross-business unit RBQM SMEs in continuous improvement and… more
    HireLifeScience (01/23/25)
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  • Merck & Co. (North Wales, PA)
    …field plus 9 years SAS programming experience in a clinical trial environment.MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering ... plus 7 or more years SAS programming experience in a clinical trial environment. Department Required Skills and Experience: Excellent interpersonal skills and… more
    HireLifeScience (12/13/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …and/or supporting dictionary up-versioning and subsequently submits requests to update company specific synonym list. Responsible for the filing of Data Management ... coding documentation and approval/signatures forms in the TMF ( Trial Master File) on an ongoing basis according to applicable Daiichi Sankyo and regulatory… more
    HireLifeScience (01/18/25)
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  • Merck & Co. (St. Louis, MO)
    …balanced, factual, scientific information about non-product areas of interest to the Company and replies to scientific questions from SLs, including questions about ... Company products. The work of an RMSD is aligned...Translational Studies Program (OTSP)-research studies.-Upon request from Global Clinical Trial Operations (GCTO):-Identify barriers to patient enrollment and retention… more
    HireLifeScience (01/22/25)
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  • Merck & Co. (Rahway, NJ)
    …art tools. With MIDD as an essential component of decision-making at our Company , this position offers an opportunity for the Pharmacometrics leader to drive ... models, quantitative system pharmacology (QSP) and disease progression models, clinical trial simulations, comparator modeling) that seek to improve cycle time,… more
    HireLifeScience (01/18/25)
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  • Merck & Co. (Rahway, NJ)
    …the art tools. With MIDD as an essential component of decision-making at our company , this position offers an opportunity for the Director to drive pipeline impact ... and pharmacodynamics (PD) analysis, model-based meta analysis (MBMA), clinical trial simulations (CTS), disease progression modeling and Artificial Intelligence… more
    HireLifeScience (01/11/25)
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  • Insmed Incorporated (Chicago, IL)
    Company DescriptionInsmed is a global biopharmaceutical company on a mission to transform the lives of patients living with serious and rare diseases. Our most ... into innovative solutions for patients. That's why we've been named the No. 1 company to work for in the biopharma industry in Science's Top Employers survey for… more
    HireLifeScience (01/16/25)
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  • Merck & Co. (Rahway, NJ)
    …PK/PD approaches, population pharmacokinetic models, exposure-response models, clinical trial design simulation, disease progression models, quantitative systems ... documents (investigational new drugs/INDs, clinical study reports (CSRs), clinical trial applications (CTDs), and representing QP2-IO at regulatory meetings.Mentoring… more
    HireLifeScience (11/26/24)
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