• Novo Nordisk Inc. (Plainsboro, NJ)
    …Are you ready to make a difference? The Position We are looking to hire an Associate Director of Clinical Operations. This is a unique opportunity to work in a ... Clinical Operations Department that manages multiple early to late-stage clinical programs. The Associate Director role will be responsible for all aspects of… more
    HireLifeScience (02/11/25)
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  • Genmab (NJ)
    …to the effective planning, and timely delivery of complete, high quality and reliable clinical trial data. The Associate Director DM will provide oversight to ... be our best, and authentic is essential to fulfilling our purpose.The Role:An Associate Director, Data Management is operationally responsible for the oversight of … more
    HireLifeScience (12/04/24)
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  • Novo Nordisk Inc. (Los Angeles, CA)
    About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... difference? The Position Drives the understanding and delivery of quality clinical research (patient safety, rights and wellbeing; data reliability; scientific… more
    HireLifeScience (02/12/25)
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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 (02/13/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionJob Overview:-We are seeking a highly qualified and experienced Associate Director in Data Management to lead our data management team in supporting ... the pharm and vaccine veterinary clinical trials. The ideal candidate will be responsible for...be responsible for overseeing the development and maintenance of clinical databases and ensuring the integrity, consistency, and confidentiality… more
    HireLifeScience (02/07/25)
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  • Genmab (Plainsboro, NJ)
    …our 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 multiple clinical trials from strategy outline through to CSR by...outline through to CSR by leading cross-functional trial specific Clinical Trial Teams (CTT) to deliver clinical more
    HireLifeScience (12/04/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Global Clinical Data Standards Vocabulary Specialist, Associate Director, is a subject matter expert in CDISC Controlled Terminology and ... growth opportunitiesThe Vocabulary Specialist may lead or participate in:Internal clinical data standards forumsStandards development teams and data governance… more
    HireLifeScience (02/11/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good ... and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and other… more
    HireLifeScience (02/11/25)
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  • The ITM Group, LLC (Daytona Beach, FL)
    …Be a clinical member of ATSA or meet the requirements for a clinical associate member Excellent verbal and written skills Ability to work independently or ... of required reports (assessments, monthly progress reports, terminations, etc.) All clinical staff members are expected to attend semi-annual staff meetings and… more
    PostJobsNow (02/07/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    … trials from protocol finalization through closeout. Relationships Reports to: Associate Director or Director of Clinical Operations. Essential Functions ... MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating a distinct R&D… more
    HireLifeScience (02/07/25)
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  • Merck & Co. (Rahway, NJ)
    …validation of Mass Spectrometry based assays that are deployed in support of clinical trials. The candidate for this Associate Principal Scientist position ... Molecular Biomarkers (TMB) is responsible for the development and execution of clinical biomarker assays across all therapeutic areas and all phases of … more
    HireLifeScience (01/30/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... aligned with the planning & successful delivery of studies within the clinical trial portfolio. Assists in creating, leading & delivering upon complex… more
    HireLifeScience (02/15/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionThe Associate Vice President (AVP)/ Metabolism Section Head in the Atherosclerosis & Metabolism Therapeutic Area within Global Clinical ... individual will be responsible for overseeing Product Development Team Leaders and- Clinical Directors within their group to ensure successful execution of programs… more
    HireLifeScience (02/12/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Job Summary: The incumbent will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in adherence to Good ... Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food...primarily a tactical study delivery role, reporting into an Associate Director (or above) responsible for Operational Study Strategy.… more
    HireLifeScience (02/05/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …areas centered around rare diseases and immune disorders. Job Summary: The Manager, Clinical Data Repository Administration is a member of the Biostatistics and Data ... maintenance of standard hierarchy structures and user access controls for all clinical studies. This position may have direct reports and/or dedicated external… more
    HireLifeScience (02/05/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating a distinct R&D ... Development Hub. Key internal stakeholders include Medical & Science, Clinical Operations, Regulatory Affairs, Data Management, Biostatistics, Non- clinical ,… more
    HireLifeScience (02/15/25)
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  • Merck & Co. (Rahway, NJ)
    …Molecular Biomarkers (TMB) is responsible for translating preclinical molecular biomarkers to clinical development across all therapeutic areas and all phases of ... clinical development at our Company's Research laboratories. TMB laboratories...biomarker leads and study teams.- The candidate for this Associate Principal Scientist position should have extensive hands-on technical… more
    HireLifeScience (02/07/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …ready to maximize your potential with us? The Position As the Associate Director of Strategic Market Insights, the functional responsibilities include leading ... sources regarding key Therapy Areas, strategic projects. Develops holistic ( clinical , commercial, managed markets), predictive landscape assessments and performs… more
    HireLifeScience (02/13/25)
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  • Genmab (Plainsboro, NJ)
    …to be our best, and authentic is essential to fulfilling our purpose.The RoleThe Associate Director of US Medical Affairs Solid Tumors Strategy will report to the ... market through collaboration with US Commercialization, Global Medical Affairs, Clinical Development, Regulatory, and other cross functional teams.This is a… more
    HireLifeScience (02/05/25)
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  • Merck & Co. (Rahway, NJ)
    …Quantitative Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical ... organization and has oversight over drug development aspects related to clinical pharmacology and pharmacometrics of oncology drugs from post-PCC to registration.… more
    HireLifeScience (01/25/25)
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