• Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …as well as other research areas centered around rare diseases and immune disorders. Summary The Director , Clinical Safety , will be a product safety lead ... specific areas of safety surveillance and risk management, and provide safety leadership including but not limited to clinical studies, post-marketing… more
    HireLifeScience (05/09/24)
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  • Merck & Co. (Rahway, NJ)
    …Action and Preventive Action (CAPAs).The incumbent ensures a single point of contact for managing clinical trial execution in all its aspects across all phases ... team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of… more
    HireLifeScience (05/10/24)
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  • Insmed Incorporated (Bridgewater, NJ)
    …Best Workplaces in New York™, and Best Workplaces for Millennials™ lists.OverviewThe Director , Clinical Development will play an important role in working ... groups.Contribute to the strategic development of early and late stage clinical programs.QualificationsRequires an MD or PharmD degree, board certified/eligible… more
    HireLifeScience (03/12/24)
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  • Merck & Co. (North Wales, PA)
    …with talented and dedicated colleagues while developing and expanding your career.The Clinical Director (Principal Scientist) has primary responsibility for the ... team. Our Company's Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of… more
    HireLifeScience (04/30/24)
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  • Tris Pharma (Monmouth Junction, NJ)
    …and team success.We have an immediate opening in our Monmouth Junction, NJ facility for a Director , Drug Safety . The Director , Drug Safety is responsible ... update reports, periodic benefit risk evaluation reports, etc.) Oversees reconciliation of safety data in pharmacovigilance and clinical trial databases Ensures… more
    HireLifeScience (04/05/24)
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  • Eisai, Inc (NJ)
    …the therapeutic area and 3 years in an in-house Medical Affairs role; MD preferredClinical research experience, including conducting clinical trials in the Phase ... If this is your profile, we want to hear from you. The Medical Director , US Medical Affairs provides medical leadership for medical affairs strategy, planning and… more
    HireLifeScience (04/26/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …known for accelerated development and approval with smaller numbers of subjects exposed, Clinical Safety and Pharmacovigilance (CSPV) must be embedded in R&D as ... possible. This led us to create the Translational Patient Safety Senior Director position, which will have...marketing. Serve as a bridge to Nonclinical Development on clinical safety findings, particularly ones likely to… more
    HireLifeScience (03/01/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …as a member of the various cross-functional forums including, Publications Planning, Clinical and Safety sub-teams, Global Brand Team, and Global Product ... areas centered around rare diseases and immune disorders.Summary The Senior Director , Global Oncology Medical Affairs is responsible for developing the Global… more
    HireLifeScience (05/07/24)
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  • Eisai, Inc (Nutley, NJ)
    …your profile, we want to hear from you. Job Summary The Medical Director will provide medical leadership for medical affairs strategy, planning and supportive ... tactics for assigned therapeutic area. Under the direction of the Senior Medical Director , this role will be responsible for working with key stakeholders to develop… more
    HireLifeScience (04/26/24)
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  • Merck & Co. (North Wales, PA)
    …and regulatory single point-of-contact for products within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS.Develops worldwide product ... Job DescriptionThe Director , Regulatory Affairs Liaison, is responsible for development and implementation of global regulatory strategy for their assigned projects… more
    HireLifeScience (04/19/24)
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  • Merck & Co. (Rahway, NJ)
    …Our company's Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of ... design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, the Director may be responsible for:-Evaluating pre- clinical and… more
    HireLifeScience (05/04/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …narratives, Provides medical direction to MW for the CSR; Working with Clinical Safety Pharmacovigilance (CSPV), defines product level surveillance plan and ... program in a specific indication, ie, multiple multinational phase II/III clinical trials; Reviews regulatory documents from cross functional, holistic perspective;… more
    HireLifeScience (03/01/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …journalsAssess clinical trial and/or other data sources to contextualize safety events for assigned product. Research natural history of disease to characterize ... centered around rare diseases and immune disorders. SUMMARYThe Associate Director , Pharmacoepidemiology position provides epidemiologic, methodological, and analytic support… more
    HireLifeScience (04/04/24)
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  • Merck & Co. (Rahway, NJ)
    …Our company's Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of ... placement, monitoring, analysis, regulatory reporting, and publication.Specifically, The Senior Director May Be Responsible For:Evaluating pre- clinical and… more
    HireLifeScience (05/04/24)
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  • Catalent (Harman, WV)
    …Supply Chain - WarehouseThe Manager, Supply Chain - Warehouse , reporting to the Director , Supply Chain, has an opportunity to make a significant impact on the way ... work onsite or at multiple sites in the Harmans, MD region.Catalent Cell & Gene Therapy hires people with...sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more… more
    HireLifeScience (05/02/24)
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  • Jazz Pharmaceuticals (Philadelphia, PA)
    …scientific background in Oncology.Expertise in the review, analysis, and interpretation of clinical -medical safety and efficacy trial data, including adverse and ... @JazzPharma on Twitter.Position Summary and Core Responsibilities:The Associate Medical Director , Jazz Oncology, Medical Affairs will support US Medical Affairs… more
    JobGet (05/12/24)
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  • Northeast Georgia Health System, Inc (Demorest, GA)
    …the Georgia Athletic Trainer Licensure Act. The certified athletic trainer performs clinical duties in accordance with population specific guidelines and adheres to ... National Patient Safety Goals as outlined in the athletic training policy...a good working rapport with students, parents, coaches, athletic director , school administration, and physicians. The athletic trainer works… more
    JobGet (05/10/24)
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  • Northeast Georgia Health System, Inc (Gainesville, GA)
    MD 's for orders (ie, medication, treatments, etc.). Shares clinical knowledge with nursing staff.Assists in coordinating admissions, transfers, or discharges ... and management of the unit nursing staff. This person manages and coordinates clinical and other activities on the unit to provide quality resident care. This… more
    JobGet (05/01/24)
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  • Director , Clinical Safety

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …well as other research areas centered around rare diseases and immune disorders. **Summary** The Director , Clinical Safety , will be a product safety lead ... safety surveillance and risk management, and provide safety leadership including but not limited to clinical...and implement strategies and action plans for identifying and managing risks throughout the product life cycle. - Effectively… more
    Daiichi Sankyo Inc. (04/30/24)
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  • Senior Medical Director -Early Oncology…

    AbbVie (North Chicago, IL)
    …and assessment) for early oncology products with a proactive approach to clinical safety , and will be interpreting regulations related to pharmacovigilance ... + Understanding and application of the pharmacology, chemistry and non- clinical toxicology to effectively conduct safety surveillance...hours in an 8 hour day) Qualifications Qualifications: + MD / DO with 2+ years of internal medicine… more
    AbbVie (03/19/24)
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