• Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines. The Associate Director is accountable for operational planning and ... quality of data is suitable for regulatory submission. The Associate Director will have routine interaction with...review and coordination for the protocol and amendments. Additional medical writing tasks may involve ICF, CRF… more
    HireLifeScience (05/18/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... and guidelines, reviews and provides written assessments of relevant medical topics, and supports PV Operations' medical ...and relevant team members.Reports and Submissions: May contribute to writing minor safety sections of the NDA, CSR, and… more
    HireLifeScience (05/14/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …implementation of sourcing strategies for a specific set of R&D categories (CRO, Medical Writing , BDM, etc..). Builds strategic plans for specific categories ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
    HireLifeScience (05/09/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... Health Authorities globally by providing input for the interaction or by writing the interaction document. May participate in meeting or teleconferences with Health… more
    HireLifeScience (04/04/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …Manager role is primarily a tactical study delivery role, reporting into an Associate Director (or above) responsible for Operational Study Strategy. This ... review & coordination for the protocol and amendments. Additional medical writing tasks may involve ICF, CRF...share with study team, Operations Program Lead, and Sr. Director for the compound, on regular basis and ensure… more
    HireLifeScience (05/22/24)
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  • Insmed Incorporated (Bridgewater, NJ)
    …study design and documentation as needed.Contribute to regulatory document writing (eg IB, IND, Integrated Summary of Immunogenicity).Engage in scientific ... pet, legal, and supplemental life insuranceFlexible spending accounts for medical and dependent careAccident and Hospital Indemnity insuranceEmployee Assistance… more
    HireLifeScience (04/23/24)
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  • Associate Director - Medical

    Novo Nordisk (Princeton, NJ)
    …The Position The Associate Director is an expert in medical writing and performs work independently with minimal-to-no supervision. The Associate ... input into development plans, study designs, and regulatory submissions. Relationships The Associate Director , Medical Writing (ADMW) reports to a … more
    Novo Nordisk (05/16/24)
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  • Associate Director , Global…

    J&J Family of Companies (Raritan, NJ)
    …the Janssen Pharmaceutical Companies. The Associate Director , Global Medical Affairs Publication Operations will provide expert writing and editing ... Associate Director , Global Medical ... Associate Director , Global Medical Affairs Publication Operations...GPP, ICMJE, and similar guidelines is preferred- Experience with medical writing document standards and processes is… more
    J&J Family of Companies (06/01/24)
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  • Associate Director , Health Economic…

    J&J Family of Companies (Titusville, NJ)
    Associate Director , Health Economic Modeling - 2406186401W **Description** Johnson & Johnson is recruiting for an Associate Director , Health Economic ... Evidence & Policy Research (SEPR) in Scientific Affairs. In this capacity the Associate Director , Economic Modeling, will design and deliver rigorous economic… more
    J&J Family of Companies (05/08/24)
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  • Associate Director , Clinical…

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    The Associate Director , Clinical Scientist leads in the development, evaluation, planning and execution of hematology oncology clinical studies and ensures ... Clinical Sciences Hematology, Clinical Sciences and collaborates closely with Medical Director (s) (MDs) to provide scientific expertise...to manage one or more clinical scientists. As an Associate Director , a typical day may include… more
    Regeneron Pharmaceuticals (04/24/24)
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  • Market Research Associate Director

    Wolters Kluwer (Trenton, NJ)
    …here. (https://youtu.be/OZ2kSzAaXK4?si=sDgZ7DZUbMnBddMq)** **What We Offer: ** The Market Research Associate Director role offers growth potential opportunities, ... benefits. **What You'll be Doing:** As our Market Research Associate Director , you will share your in-depth...skills and meticulous attention to detail + Excellent professional writing and communication skills + Proficiency in MS Office… more
    Wolters Kluwer (04/27/24)
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  • Associate Director , Autologous Cell…

    J&J Family of Companies (Raritan, NJ)
    Associate Director , Autologous Cell Therapy Process Development - 2406176241W **Description** Johnson & Johnson is currently seeking an Associate Director ... We are seeking an energetic and highly motivated candidate for the role of Associate Director , who possesses proven expertise in autologous cell therapy process… more
    J&J Family of Companies (06/05/24)
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  • Associate Director , Global Labeling…

    J&J Family of Companies (Titusville, NJ)
    Associate Director , Global Labeling Product Leader - 2406187352W **Description** Johnson & Johnson Innovative Medicine is recruiting for an Associate ... Relevant experience in the pharmaceutical industry (eg, Regulatory Affairs, Clinical, Medical Information, Pharmacovigilance) including at least 6 years of direct… more
    J&J Family of Companies (05/11/24)
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  • Associate Director , Combination…

    Merck (Trenton, NJ)
    … Device and Combination Product (MDCP) Quality Assurance Operations team, the Associate Director Quality Engineering & Quality Assurance is responsible for ... independent compliance support of Medical Devices including the device constituent part of Combination...a cross functional framework and will involve detailed technical writing and review. + A high degree of creative… more
    Merck (05/31/24)
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  • Associate Director , US Oncology…

    Bristol Myers Squibb (Princeton, NJ)
    …integral member of the US Hematology & Oncology Commercial Communications team. The Associate Director , US Oncology Communications will support both brand and ... A strategic communications background in healthcare (eg pharma, agency, non-profit, academic medical center) is strongly preferred. + A strong commercial focus and… more
    Bristol Myers Squibb (04/10/24)
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  • Associate Director , Biostatistics

    System One (Basking Ridge, NJ)
    Job Title: Associate Director , Biostatistics Client - Global Pharmaceutical Company Location: Remote, US Based only - must reside in EST or CST time zones Type: ... Health Authorities globally by providing input for the interaction or by writing the interaction document. May participate in meeting or teleconferences with Health… more
    System One (05/13/24)
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  • Associate Director

    Bristol Myers Squibb (Princeton, NJ)
    …and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , Commercialization Communications supports the development and ... and the overall healthcare environment. This individual must have superior writing skills and a track record of delivering executive communication materials.… more
    Bristol Myers Squibb (05/16/24)
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  • Associate Director , Clinical Safety…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... and guidelines, reviews and provides written assessments of relevant medical topics, and supports PV Operations' medical ...team members. + Reports and Submissions: May contribute to writing minor safety sections of the NDA, CSR, and… more
    Daiichi Sankyo Inc. (05/15/24)
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  • Associate Director , R&D Procurement…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …implementation of sourcing strategies for a specific set of R&D categories (CRO, Medical Writing , BDM, etc..). Builds strategic plans for specific categories ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
    Daiichi Sankyo Inc. (05/09/24)
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  • Associate Director , Biostatistics…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... Health Authorities globally by providing input for the interaction or by writing the interaction document. May participate in meeting or teleconferences with Health… more
    Daiichi Sankyo Inc. (05/24/24)
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