• Merck & Co. (Rahway, NJ)
    …company is seeking a highly motivated candidate for the position of Director , Small Molecule Development within the Mixed Modalities, Sterile Product Development ... for parenteral drug products within the small molecule and synthetic modality pipeline.The Director will report to the Executive Director of Sterile Product… more
    HireLifeScience (10/11/24)
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  • Merck & Co. (Rahway, NJ)
    …portfolio. Within Biologics and Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team ... opportunity is fast paced and contributes to the Pharmaceutical Sciences and Clinical Supplies (PSCS) deliverable which is the development of robust compositions,… more
    HireLifeScience (10/08/24)
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  • Merck & Co. (Rahway, NJ)
    …labeling and obtain shortest time to approval by global regulatory agencies.Reports to Associate Vice President, Executive Director , or Senior Director in ... Job DescriptionWe are seeking a Director (Principal Scientist), Global Regulatory Affairs Liaison with...our company; where no regulatory guidance exists; where the program is accelerated; has an external business partner; there… more
    HireLifeScience (10/09/24)
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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 (09/08/24)
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  • Eisai, Inc (Nutley, NJ)
    …we want to hear from you.The Northeast Region covers NJ, PA, & DE.The Associate Director , Regional Thought Leader Liaison (RTLL), AD Marketing will lead and ... promotional speakers and related aspects of speaker programsCollaborate with Promotional Program Manager for speaker usage and issuesOffer feedback on nominating new… more
    HireLifeScience (10/17/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …as the Clinical Safety Scientist Lead for a large, late-stage program or multiple early-stage programs, in order to proactively perform safety surveillance and ... as the Clinical Safety Scientist Lead for a large, late-stage program or multiple early-stage programs, in order to proactively perform safety surveillance and… more
    HireLifeScience (10/18/24)
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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 (10/18/24)
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  • Legend Biotech USA, Inc. (Piscataway, NJ)
    …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Associate Director Immuno-Oncology as part of the Research and Development ... cell-based therapies. We are seeking an experienced and dynamic Associate Director to lead our in vivo... to lead our in vivo CAR-T cell therapy program . If you're passionate about advancing groundbreaking treatments and… more
    HireLifeScience (07/26/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …other research areas centered around rare diseases and immune disorders. Summary: The Associate Director will lead the execution and lifecycle management of ... Global Medical Affairs' externally sponsored clinical research (ESR) initiatives, ensuring strict adherence to Good Clinical Practices (GCPs), relevant Standard… more
    HireLifeScience (09/24/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …to CDx project teams for the diagnostic, under the direction of the Global Program Teams (GPT) CDx representative for the therapeutic or under the guidance of the ... and technical expertise by collaborating closely with Translational Science Leads, Clinical Biomarker Leads, Biosample Operations, Clinical Leads and Regulatory… more
    HireLifeScience (09/25/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …aligned therapeutic / franchise area(s). Relationships Reports to the Senior Director of Value Communication and Contracting Strategy. Interacts frequently in ... pricing scenarios and strategy for all pipeline products starting in Phase II clinical trials Leads assessment of investments in payer contracts and patient copay… more
    HireLifeScience (10/05/24)
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  • Associate Director , Program

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …(s) for Clinical Data Management (CDM). + Maintains an overview of clinical program (s) status and issues and proactively communicates progress, risks, issues ... might be for you if can:** + Acts as point of contact for clinical program and study level escalation. + Reviews key metrics and Key Performance Indicators… more
    Regeneron Pharmaceuticals (10/18/24)
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  • Clinical Assistant/ Associate

    Fairleigh Dickinson University (Teaneck, NJ)
    Job Summary: Clinical Assistant/ Associate Professor & Clinical Director , Physician Assistant Program will develop, maintain, and ensure adequacy and ... assisting in the accreditation efforts for the physician assistant program , working with the Program Director.... This position, non-tenured and at the rank of clinical assistant or associate professor, serves as… more
    Fairleigh Dickinson University (08/06/24)
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  • Program Director

    Touro University (New York, NY)
    …The Program Director and Associate Professor the master's program in Clinical Mental Health Counseling is expected to support our growing student ... Overview MS in Clinical Mental Health Counseling program at...Health Sciences invites applications for a full-time position as Program Director and Associate (or… more
    Touro University (08/08/24)
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  • Associate Director , Clinical

    Merck (Rahway, NJ)
    clinical development teams and the operational/executional arms within the business. The Program Clinical Supplies Project Manager ( Program CSPM) serves ... spokesperson at clinical and development related meetings. Working independently, the Program CSPM designs strategic and operational plans for all clinical more
    Merck (10/12/24)
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  • Associate Director , Clinical

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …ensures scientific integrity and interpretation of study data of a clinical development program . The Associate Director leads in a matrix environment as ... join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads...may include the following: + May function as lead Clinical Scientist for program , and/or as delegate… more
    Regeneron Pharmaceuticals (10/10/24)
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  • Associate Director , Clinical

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …ensures scientific integrity and interpretation of study data of a clinical development program . The Associate Director leads in a matrix environment as ... to join our Clinical Development team. The Associate Director Clinical Sciences leads...may include the following:** + May function as lead Clinical Scientist for program , and/or as delegate… more
    Regeneron Pharmaceuticals (09/19/24)
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  • Associate Director , Clinical

    Regeneron Pharmaceuticals (Tarrytown, NY)
    The Associate Director , Clinical Sciences contributes to the development, evaluation, planning and execution of hematology clinical studies and ensures ... scientific integrity and interpretation of study data of a clinical development program . Works in a matrix...on clinical studies and programs. As an Associate Director , a typical day may include… more
    Regeneron Pharmaceuticals (10/16/24)
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  • Associate Director , Clinical

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …as the Clinical Safety Scientist Lead for a large, late-stage program or multiple early-stage programs, in order to proactively perform safety surveillance and ... as the Clinical Safety Scientist Lead for a large, late-stage program or multiple early-stage programs, in order to proactively perform safety surveillance and… more
    Daiichi Sankyo Inc. (10/19/24)
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  • Associate Director , Clinical

    Daiichi Sankyo Inc. (Basking Ridge, 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
    Daiichi Sankyo Inc. (10/19/24)
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