• Daiichi Sankyo, Inc. (Bernards, NJ)
    …and globally, and provide legal support for licensing, co-promotion, co-development, clinical trial collaboration, co-marketing and acquisition agreements (among ... in negotiating, drafting and reviewing licensing, co-promotion, co-development, co-marketing, clinical trial collaboration, companion diagnostic, and acquisition… more
    HireLifeScience (09/26/25)
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  • Merck & Co. (Rahway, NJ)
    …Atherosclerosis, Cardiology Clinical Research, Cardiovascular Diseases, Clinical Development, Clinical Studies, Clinical Trial Designs, Clinical ... Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the… more
    HireLifeScience (10/07/25)
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  • Merck & Co. (Rahway, NJ)
    …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 (09/30/25)
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  • Merck & Co. (Rahway, NJ)
    …field and relevant experienceRequired Experience and Skills:-- -A deep understanding of the clinical trial process: You can speak the language of protocols, ... Job DescriptionWe are seeking an Associate Principal Scientist to contribute to a pivotal...stewarding these data, you will empower our scientists and clinical teams to make faster, data-driven decisions that propel… more
    HireLifeScience (10/01/25)
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  • Eisai, Inc (Nutley, NJ)
    …and other international regulatory/ethical guidelines relevant to the pharmaceutical industry & clinical trial conduct, and to ensure compliance with these ... If this is your profile, we want to hear from you. The Associate Director/Director, MSLs is responsible for the leadership, direction and management of MSLs… more
    HireLifeScience (10/07/25)
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  • Eisai, Inc (Nutley, NJ)
    …country strategic development, planning, implementation, and oversight of Phase I through IV clinical trial programs and early new product development within the ... Medical Affairs department for assigned product(s). The Associate Medical Director utilizes expert medical, clinical and scientific knowledge in assigned… more
    HireLifeScience (09/05/25)
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  • Clinical Trial Associate

    Actalent (Parsippany Troy Hills, NJ)
    The Clinical Trial Assistant plays a crucial role in supporting clinical trial coordination and implementing clinical operational plans in line with ... + 3-5 years of experience in the biotech industry and clinical drug development or trial execution. + Advanced skills in Microsoft Office and knowledge of… more
    Actalent (10/10/25)
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  • Associate Director, TAIP Principal Analyst…

    Bristol Myers Squibb (Princeton, NJ)
    …decision-making throughout execution. You will apply a strong foundation in both clinical trial science and applied analytics - from understanding protocol ... or trial strategy is required + Prior exposure to clinical trial delivery processes and data-driven decision making + Strong therapeutic area knowledge… more
    Bristol Myers Squibb (10/11/25)
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  • Clinical Trial Navigator

    Actalent (Princeton, NJ)
    Remote Clinical Research Nurse Job Description We are seeking a Remote Clinical Trial Navigator to support clinical research sites, particularly in the ... with site-level staff. + Utilize Interactive Response Technology (IRT) to manage clinical trial logistics. + Engage in prescreening and reviewing portals… more
    Actalent (10/08/25)
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  • Associate Director, Strategy…

    Bristol Myers Squibb (Princeton, NJ)
    …alignment with corporate objectives through three crucial pillars: unifying the Trial Delivery Support (TDS) organization and streamlining ways of working, bringing ... medicines to patients faster. This position reports directly to the President of Trial Delivery Support and provides key support to the TDS leadership team 1.… more
    Bristol Myers Squibb (10/03/25)
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  • Associate Clinical Project…

    IQVIA (Parsippany, NJ)
    **Position Overview:** IQVIA is seeking an experienced Associate Clinical Project Management Director/ Trial Delivery Manager (TDM) to lead and coordinate ... global and regional clinical trial management activities. This role ensures the successful planning, execution, and closure of clinical trials, whether… more
    IQVIA (10/09/25)
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  • Associate Director Clinical

    Actalent (New York, NY)
    …Location of Candidate: Open to remote Candidates in EST Job Description Manage clinical trial activities for multiple trials, ensuring the timely completion of ... Job Title: Associate Director, Clinical Operations Company: Small...for assigned clinical trials. Responsibilities + Manage clinical trial activities for multiple trials, ensuring… more
    Actalent (10/10/25)
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  • Associate Director, Product Manager…

    Bristol Myers Squibb (Princeton, NJ)
    …15+ years of demonstrable experience in pharmaceutical industry with proven expertise in clinical trial execution, data acquisition, and analysis reporting on a ... quality, data products, and analytic ready data solutions for GDD Clinical Intelligence ( Trial Simulation & Modeling, Clinical Data Review, Programming and… more
    Bristol Myers Squibb (10/10/25)
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  • Associate Director, Clinical Science

    Bristol Myers Squibb (Princeton, NJ)
    … development, the position is responsible for various aspects of ongoing clinical trial program-related activities within the relevant therapeutic area. These ... their personal lives. Read more: careers.bms.com/working-with-us . **Summary** The Associate Director of Clinical Science plays a...may be assigned. + Acquires and utilizes knowledge of clinical trial design to develop or oversee… more
    Bristol Myers Squibb (09/17/25)
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  • Associate Director, Neuroscience,…

    Bristol Myers Squibb (Princeton, NJ)
    …oncology, immunology, cardiovascular and neuroscience. This group integrates laboratory science, clinical trial /biomarkers and asset development as well as ... stage drug development and activities required for and related to clinical trial initiation, maintenance and completion + Strong verbal and written communication… more
    Bristol Myers Squibb (10/04/25)
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  • (Senior) Clinical Research Associate

    IQVIA (Parsippany, NJ)
    …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. *… more
    IQVIA (07/14/25)
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  • Clinical Research Associate

    IQVIA (Parsippany, NJ)
    …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... in accordance with contracted scope of work and Good Clinical Practice. * Work with sites to adapt, drive,...required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's… more
    IQVIA (09/19/25)
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  • Associate Director, Strategic Sourcing,…

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …R&D categories including data management, diagnostics, patient platforms, site management and clinical trial support suppliers across all phases of development. ... The Associate Director, Strategic Sourcing, Clinical Category Lead, will lead the Strategic Sourcing efforts for… more
    Otsuka America Pharmaceutical Inc. (09/05/25)
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  • Spring 2026 Co-Op Early Clinical

    Bristol Myers Squibb (Princeton, NJ)
    …their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Clinical Scientist/ Clinical Science co-op function ... oncology and cellular therapies. + Supports execution of assigned clinical trial activities and works closely with...study-related documents. + Support the development of site and Clinical Research Associate (CRA) training materials. +… more
    Bristol Myers Squibb (10/04/25)
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  • Senior Manager, Clinical Data Management

    Bristol Myers Squibb (Madison, NJ)
    …projects + Efficiently plans, coordinates, and delivers complete, high quality and reliable clinical trial data in a timely manner for assigned projects + ... BMS R&D pipeline. This role may report into Director, Clinical Data Management or Associate Director, ...functional study team members to ensure on-going review of trial data currency, quality and completeness + Represents DM… more
    Bristol Myers Squibb (10/10/25)
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