• Daiichi Sankyo, Inc. (Bernards, NJ)
    …research areas centered around rare diseases and immune disorders. JOB SUMMARYThe Senior Director , Head Medical affairs Quality Assurance in Global RD/PV ... of a quality strategy and quality plan closely aligned with the Global Oncology Medical Affairs (GOMA), Oncology Business Unit (OBU) and Specialty Business Unit… more
    HireLifeScience (04/25/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... working with contract manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub team and the RA… more
    HireLifeScience (05/15/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    … trial and screen failures. Clinical trial protocol development and reviews ( clinical trial protocols and medical device protocols)ICF reviews to ensure ... 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 (05/29/25)
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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 ... to regulatory agencies. Supervise designated personnel. Relationships Report to the Director Regulatory Affairs . Develop and maintain positive rapport and… more
    HireLifeScience (06/06/25)
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  • Merck & Co. (Boston, MA)
    …in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; and assist the Executive Director and/or ... Atherosclerosis & Metabolism medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the entire… more
    HireLifeScience (06/07/25)
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  • Merck & Co. (Boston, MA)
    …and will interact externally with key opinion leaders.-Specifically, the Executive Director may be responsible for:Evaluating pre- clinical and translational work ... opportunities.Managing other Directors and/or Senior Directors responsible for Atherosclerosis clinical development projectsThe Executive Director may supervise… more
    HireLifeScience (06/07/25)
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  • Merck & Co. (New York, NY)
    Job DescriptionOur Medical Affairs team advances patient care by engaging in scientific exchange with external medical experts and industry professionals ... Clinical Practice (GCP), Hospital Medicine, Immuno-Oncology, Immunotherapy, Management Process, Medical Affairs , Medical Knowledge, Oncology, Oncology… more
    HireLifeScience (06/03/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Sankyo. The candidate will collaborate globally with Formulation and Analytical Scientists, Clinical Operations, Regulatory Affairs CMC, and Clinical ... 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 (05/18/25)
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  • Eisai, Inc (Raleigh, NC)
    At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care ... If this is your profile, we want to hear from you. The Director Western Supply Chain Management (SCM) Unit is accountable and/or responsible for providing… more
    HireLifeScience (05/07/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …and technical QA oversight.Drive innovative process improvements across RD, PV, and Medical Affairs by leveraging emerging technologies and industry best ... centered around rare diseases and immune disorders. SummaryThe Sr. Director , Data Quality and Integrity (Global R&D & PV...drive harmonization of systems specific to RD, PV, and Medical Affairs .Oversee and ensure the deliverables of… more
    HireLifeScience (06/02/25)
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