• Genmab (Plainsboro, NJ)
    …as Clinical Drug Supply Manager, of the following tasks:Global Clinical Drug Supply Project/ Trial ManagementObtain Project/ Trial specific information ... possible mitigations (contingency plans and new/additional scenarios) that may impact clinical drug supply)Create and maintain program/project and trial IMP/AMP… more
    HireLifeScience (01/07/25)
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  • Genmab (Plainsboro, NJ)
    …Planning and Operational ExecutionOversee strategic and operational plans for clinical trial drug supply.Maintain agreements, contracts, and SOPs ... You are skilled in professional and clear written and oral communication to ensure activities are carried out as...or biopharmaceutical industry.Broad and Diverse experience in working with trial management for global clinical drug supply… more
    HireLifeScience (01/07/25)
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  • Merck & Co. (Rahway, NJ)
    …optimal trial design and monitoring of studies, producing high-quality clinical documents and presentations. The position requires a solid understanding of the ... Head in the Atherosclerosis & Metabolism Therapeutic Area within Global Clinical Development will focus on driving strategy, development, and life-cycle management… more
    HireLifeScience (02/12/25)
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  • Genmab (Plainsboro, NJ)
    …you will 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 ... others.You will join a highly competent global team focused on packaging and labeling clinical trial supplies, collaborating closely with the Global Clinical more
    HireLifeScience (12/19/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …Strong understanding of market needs and resource allocation Strong expertise in clinical trial methodology and conduct, and GCP principles Superior ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...most diverse and collaborative groups within the organization. From health- care -provider interactions and developing and implementing regulatory strategies with… more
    HireLifeScience (02/01/25)
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  • Merck & Co. (Rahway, NJ)
    …or related field plus 9 years SAS/R programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life ... related field plus 7 or more years SAS/R programming experience in a clinical trial environmentRequired Experience and Skills: Excellent interpersonal skills and… more
    HireLifeScience (01/09/25)
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  • Merck & Co. (Rahway, NJ)
    …Global Clinical Supplies, Global Quality, Global Regulatory Affairs, Global Clinical Trial Operations, Device Development and our Research & Development ... and is responsible for oversight of manufacturing activities for the Clinical Supply Chain. Partnering across our internal facilities and external contract… more
    HireLifeScience (02/13/25)
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  • Merck & Co. (Rahway, NJ)
    …and associated regulatory submissions for Investigational New Drug applications and Clinical Trial Applications.Duties may include, but are not limited ... procedures, and to provide independent assurance that delivers high quality data and clinical supplies. This position reports to the Associate Director of Global … more
    HireLifeScience (02/11/25)
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  • Merck & Co. (North Wales, PA)
    …or related field plus 9 years SAS programming experience in a clinical trial environment.MS in Computer Science, Statistics, Applied Mathematics, Life ... related field plus 7 or more years SAS programming experience in a clinical trial environment. Department Required Skills and Experience: Excellent interpersonal… more
    HireLifeScience (12/13/24)
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  • Merck & Co. (Rahway, NJ)
    …development and qualification of release, characterization, and stability assays for testing of clinical trial material and in support of product and process ... and data interpretation.- Applicants must have effective organizational, multi-tasking, oral /written communications skills, show scientific leadership, and a desire… more
    HireLifeScience (02/15/25)
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  • Lundbeck (Dallas, TX)
    …trials (IIT) aligned with Lundbeck's medical strategies Upon request, assists in clinical trial and research efforts by recommending qualified investigators and ... and support Fulfills unsolicited requests for medical information from health care professionals Actively participates in executing Lundbeck's strategy at scientific… more
    HireLifeScience (01/28/25)
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  • Genmab (Plainsboro, NJ)
    …the value of assigned asset(s),Provide strategic market access input to inform global clinical development program of assigned asset(s) and ensure it is optimized to ... meet the needs of global payers (eg, relevant endpoints, trial design, sub-populations, evidence of cost offsets) by incorporating HTA and payers' perspectives… more
    HireLifeScience (02/05/25)
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  • Merck & Co. (South San Francisco, CA)
    …disease targets in discovery, being innovative and foreseeing the path to clinical trial .Leverage scRNASeq to contextualize target gene expression in the ... space.- Your work will inform discovery, translational medicine, companion diagnostics and clinical research.You will serve as a strategic partner to our discovery… more
    HireLifeScience (01/25/25)
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  • Senior Manager, Clinical Trial

    Bristol Myers Squibb (Princeton, NJ)
    …professional who has a strong proficiency in the curation and analysis of clinical trial intelligence data and its application to effectively conduct study ... and the creation/maintenance of data-driven patient recruitment and enrollment forecasts for clinical trial (s) within a clinical research development… more
    Bristol Myers Squibb (02/17/25)
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  • Delivery Manager ( Clinical Trial

    Actalent (Chicago, IL)
    Description: Actalent is currently hiring for a Delivery Manager - Clinical Trial Management role. This is a permanent leadership position. Here are some key ... brochures and other regulatory documents, as required * Ensure clinical trial master file for assigned trials...is an asset * Must have strong written and oral communication skills and Experience mentoring/coaching and providing training… more
    Actalent (02/04/25)
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  • Associate Medical Director, Innovative…

    AbbVie (North Chicago, IL)
    …experience in drug safety or a related discipline in the pharmaceutical industry + Clinical trial experience strongly preferred + Excellent clinical judgment ... lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For… more
    AbbVie (12/19/24)
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  • Clinical Trials Specialist

    University of Washington (Seattle, WA)
    …Union. The CTS reports to the Senior Research Implementation Manager and Lead Clinical Trial Specialist. This position interacts closely with multiple process ... Medicine. The Division's primary mission is to improve cancer care by moving discoveries made in the laboratory to...and external academic institutions. The CTS is responsible for clinical trial study start up in the… more
    University of Washington (01/01/25)
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  • Advanced Clinical Social Worker (Part-Time)

    State of Connecticut, Department of Administrative Services (New Haven, CT)
    …managed at CMHC. + Works with the director of SIERRA to potentially screen for clinical appropriateness and level of mental health care that would be needed. + ... person for communication between CMHC CFS team and SIERRA Pre- Trial . About Us: DMHAS is a health care...clinical social worker practice standards; + Considerable + oral and written communication skills; + administrative skills; +… more
    State of Connecticut, Department of Administrative Services (01/24/25)
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  • Scientific Director, Clinical Development…

    AbbVie (Irvine, CA)
    …understanding of relevant therapeutic area is required. Knowledge of clinical trial methodology coupled with performance in eye care registration enabling ... significant leadership responsibilities and practical experience in successful eye care registration trial programs is especially important....those in development by AbbVie or with AbbVie eye care clinical partners is very desirable. +… more
    AbbVie (01/10/25)
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  • Medical Director Clinical Development Eye…

    AbbVie (Irvine, CA)
    …Completion of a subspecialty fellowship is desirable. + At least 2 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent. + ... key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan...a global scientific and business strategy. + Knowledge of clinical trial methodology, regulatory and compliance requirements… more
    AbbVie (02/13/25)
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