• Merck & Co. (Rahway, NJ)
    Job DescriptionPosition Description: Associate Director , Clinical Scientist This position drives scientific planning, strategy and execution of Phase 1-4 ... execution of clinical protocol(s).Serves as the lead clinical scientist on the clinical ... clinical data/medical protocol-deviations in collaboration with the Clinical Director .Builds talent and capabilities of direct… more
    HireLifeScience (11/05/24)
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  • Merck & Co. (Rahway, NJ)
    …talented and dedicated colleagues while developing and expanding your career.The Senior Director (Senior Principal Scientist ) has primary responsibility for the ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will...safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipation in internal more
    HireLifeScience (11/08/24)
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  • Merck & Co. (Rahway, NJ)
    …talented and dedicated colleagues while developing and expanding your career.-- The Director (Principal Scientist ) has primary responsibility for the planning ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage...safety and efficacy as well as new drug applications, clinical study reports, or publication; andParticipation in internal more
    HireLifeScience (11/08/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionWe are seeking a Director (Principal Scientist ), Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can help advance ... our pipeline and drive our strategic priorities.The Director , Principal Scientist - Regulatory Affairs Liaison is responsible for development and implementation… more
    HireLifeScience (10/31/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionWe are seeking a Senior Director (Sr. Principal Scientist ) Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can ... and drive our strategic priorities.Summary, Focus and PurposeThe Senior Principal Scientist - Regulatory Affairs Liaison is responsible for development and… more
    HireLifeScience (10/31/24)
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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 (11/08/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …areas centered around rare diseases and immune disorders.SummaryThis position serves as the Clinical Safety Scientist Lead for a large, late-stage program or ... Risk Management (Signal identification, evaluation, mitigation):This position serves as the Clinical Safety Scientist Lead for a large, late-stage program… more
    HireLifeScience (10/18/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    Director Safety Surveillance, US East Coast Development Hub. Key internal stakeholders include Medical & Science, Clinical Operations, Regulatory Affairs, ... and Seattle reflect the full R&D continuum, from early research through late-stage clinical development. Here, we are building for the future, creating a distinct… more
    HireLifeScience (09/13/24)
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  • Director , Clinical Scientist

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …through early and/or late phase development. The Director reports to the Internal Medicine Clinical Development Unit Lead of Clinical Scientists and ... are seeking a Director to join our Clinical Development team. The Director Clinical...may include the following:** + May function as lead Clinical Scientist for program, and/or as delegate… more
    Regeneron Pharmaceuticals (09/17/24)
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  • Associate Director , Clinical

    Regeneron Pharmaceuticals (Tarrytown, NY)
    … to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution ... scientific integrity and interpretation of study data of a clinical development program. The Associate Director 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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  • Director , Clinical Scientist

    Regeneron Pharmaceuticals (Tarrytown, NY)
    … Sciences, a typical day may include the following:** + May function as lead Clinical Scientist for program, and/or as delegate of Therapeutic area Lead ... The Director , Clinical Sciences, Oncology leads in the development,...Clinical Scientist + Guides assigned Program team(s)/direct reports and… more
    Regeneron Pharmaceuticals (10/10/24)
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  • Associate Director , Clinical

    Regeneron Pharmaceuticals (Tarrytown, NY)
    Director , a typical day may include the following: + May function as Clinical Scientist for program, and/or as delegate of Therapeutic area Clinical ... The Associate Director , Clinical Sciences contributes to the...Presents data and information to external investigators (SIV) and internal collaborators + Proficient analytical knowledge and skills to… more
    Regeneron Pharmaceuticals (10/16/24)
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  • Director , Oncology Early Stage…

    Pfizer (New York, NY)
    **ROLE SUMMARY:** The overall role of the Oncology Early Stage Clinical Scientist (ESCS) is to lead and coordinate the development of multiple studies for novel ... through proof-of concept + Serve as technical resource for clinical issues raised by internal and external... clinical development issues. + The Early Stage Clinical Scientist may lead the development of… more
    Pfizer (11/08/24)
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  • Associate Director , Clinical

    Merck (Rahway, NJ)
    **Job Description** **Position Description:** **Associate Director , Clinical Scientist ** This position drives scientific planning, strategy and execution of ... clinical protocol(s). + Serves as the lead clinical scientist on the clinical ...clinical data/medical protocol deviations in collaboration with the Clinical Director . + Builds talent and capabilities… more
    Merck (11/05/24)
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  • Associate Director , Clinical Safety…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …around rare diseases and immune disorders. **Summary** This position serves as the Clinical Safety Scientist Lead for a large, late-stage program or multiple ... Management (Signal identification, evaluation, mitigation):** + This position serves as the Clinical Safety Scientist Lead for a large, late-stage program or… 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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  • Director , Global Regulatory Affairs…

    Merck (Rahway, NJ)
    **Job Description** We are seeking a Director (Principal Scientist ), Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can help ... advance our pipeline and drive our strategic priorities. The Director , Principal Scientist | Regulatory Affairs Liaison is responsible for development and… more
    Merck (10/31/24)
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  • Associate Director , US Medical Promotional…

    Bristol Myers Squibb (Madison, NJ)
    …personal lives. Read more: careers.bms.com/working-with-us . **Position:** Associate Director , Medical Promotional Review Scientist , Neuropsychiatry ... **Location:** Princeton Pike, NJ or Madison, NJ The Associate Director , Medical Promotional Review Scientist plays a critical role in the Medical Strategy team.… more
    Bristol Myers Squibb (10/03/24)
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  • Senior Principal Scientist (Senior…

    Merck (Rahway, NJ)
    **Job Description** We are seeking a Senior Director (Sr. Principal Scientist ) Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that ... our strategic priorities. **Summary, Focus and Purpose** The Senior Principal Scientist | Regulatory Affairs Liaison is responsible for development and… more
    Merck (10/31/24)
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  • Translational Medicine Sr. Principal…

    Bristol Myers Squibb (Summit, NJ)
    …pioneer. Join us and make a difference. **Summary/Scope** Reporting to Senior Scientific Director Translational Medicine, the TM Sr. Principal Scientist will be ... group. The individual will be responsible for TM and clinical biomarker activities to support drug development programs in...and analysis and associated timelines by working with relevant internal functions and CROs; + Prepares and delivers … more
    Bristol Myers Squibb (09/23/24)
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