• Merck & Co. (Rahway, NJ)
    …team members including clinical directors and study managers to lead/support clinical trial scientific activities in the Atherosclerosis & Metabolism TA.Job ... of clinical protocol(s). Serves as the lead clinical scientist on the clinical trial...clinical data/medical protocol deviations in collaboration with the Clinical Director .Builds talent and capabilities of direct/indirect… more
    HireLifeScience (11/13/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to ... leader (CSL)Study Planning and Execution: Provides input on major milestones of trial , clinical trial plan and contingency planning; Analyzes and updates… more
    HireLifeScience (11/12/24)
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  • Genmab (Plainsboro, NJ)
    …as trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and ... to be our best, and authentic is essential to fulfilling our purpose.The RoleThe Associate Director acts as a statistical expert supporting the clinical more
    HireLifeScience (10/18/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …actual product Responsible for all areas related to patient safety in clinical trials Act as member of the trial safety group for dose escalation decisions ... external stakeholders. Relationships This position will report to Senior Director Safety Surveillance, US East Coast Development Hub. Key...) Provide safety input to Product Development Plan (PDP), Trial Outline, Protocol, Clinical Trial more
    HireLifeScience (09/13/24)
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  • Merck & Co. (North Wales, PA)
    …/Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review and approval of all US ... for anticipated promotional messages and claims (aligned with marketing strategy) in clinical trial design and product labeling as it relates to the use of… more
    HireLifeScience (11/15/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …research areas centered around rare diseases and immune disorders. Summary The Associate Director Global Oncology Strategic Planning provides strategic insights ... are tracked and ensure implications are assessed and communicated on timely manner- Clinical Development Life Cycle Management Decision Support: Be the key point of… more
    HireLifeScience (09/24/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …preferred Experience- 7 or More Years Outsourcing, health sciences or related field ( clinical trials ) required- 7 or More Years Deep experience in pharma ... & category management required- CRO experience preferred- Strong knowledge of clinical trials preferred- Demonstrated ability to leverage digital data… more
    HireLifeScience (09/24/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating a distinct R&D ... across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions Serve as a member… more
    HireLifeScience (09/17/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …and leads technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing ... laboratory members, the Contract Manufacturing Organization (CMO), Labeling members and Clinical members. This position works with non-standard problems of some… more
    HireLifeScience (11/17/24)
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  • Genmab (Plainsboro, NJ)
    …and/or leading a small team to complete various programming efforts within a clinical trial .You will be responsible for ensuring integrity, consistency, and ... Director , Programming, and work closely with Data Management, Clinical Programming, Statistics, Medical Writing, and other functions as necessary.Position level… more
    HireLifeScience (10/11/24)
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  • Eisai, Inc (Louisville, KY)
    …with internal cross functional partners including but not limited to Associate Director Regional Marketing, Oncology Field Reimbursement Managers, and ... customer business, disease state, product prescribing information, approved promotional clinical trials , patient access to medication, and regulatory/compliance… more
    HireLifeScience (10/19/24)
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  • Eisai, Inc (San Francisco, CA)
    …with internal cross functional partners including but not limited to Associate Director Regional Marketing, Oncology Field Reimbursement Managers, and ... customer business, disease state, product prescribing information, approved promotional clinical trials , patient access to medication, and regulatory/compliance… more
    HireLifeScience (10/17/24)
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  • Associate Director , Clinical

    Regeneron Pharmaceuticals (Tarrytown, NY)
    Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, ... scientific integrity and interpretation of study data of a clinical development program. The Associate Director...clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments + Authors… more
    Regeneron Pharmaceuticals (10/10/24)
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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 ... on clinical studies and programs. As an Associate Director , a typical day may include...clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments. Authors and/or… more
    Regeneron Pharmaceuticals (10/16/24)
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  • Hem Onc, Associate Director

    University Of Vermont (Burlington, VT)
    …Posting Number F2924PO Department Med-Hematology Oncology/55538 Advertising/Posting Title Hem Onc, Associate Director Clinical Translational Research- ... Center is seeking a physician-scientist/academic clinician to serve as Associate Director of Clinical &...by a history of peer-reviewed publications, extramural funding and/or clinical trials activity. Burlington is a vibrant… more
    University Of Vermont (09/18/24)
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  • Associate Director - Clinical

    Lilly (Indianapolis, IN)
    …to ensure technology enables clinical trial design and execution. The Associate Director , Clinical Supply Systems, will ensure timely delivery of ... oversight, and management of clinical processes, information, and technologies within Clinical Trial Foundations (CTF) organization, Clinical Supply and… more
    Lilly (10/30/24)
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  • Scientific Associate Director

    Amgen (South San Francisco, CA)
    …patients worldwide. It's time for a career you can be proud of. **Scientific Associate Director - Clinical Pharmacology, Modeling & Simulation** **Live** ... data science and predictive analytics to support drug development. The Scientific Associate Director will also work collaboratively with other functional areas… more
    Amgen (11/30/24)
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  • Associate Director , Clinical

    Gilead Sciences, Inc. (Foster City, CA)
    …their aspirations. Join Gilead and help create possible, together. **Job Description** ** Associate Director , Clinical Pharmacology - Oncology** **_*This is ... with regulatory agencies. + Anticipates problems that may arise in clinical trials and develops solutions for these using precedents and original thinking.… more
    Gilead Sciences, Inc. (11/26/24)
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  • Associate Director - Clinical

    Lilly (Indianapolis, IN)
    trials globally for all business units across all phases of development. The Associate Director (P4), Clinical Central Services, and Innovation (CCSI) ... + Collaborate with key stakeholders (ie , Quality, Privacy, Legal, Tech@Lilly, Procurement, Clinical Trial Foundations) in support of the portfolio​​. + Manage… more
    Lilly (11/28/24)
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  • Associate Director , Global…

    Teva Pharmaceuticals (West Chester, PA)
    Associate Director , Global Clinical Quality Date: Nov 21, 2024 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job ... and regulations, supports risk management activities, and leads continuous improvement for clinical development activities. The Associate Director - Global… more
    Teva Pharmaceuticals (11/22/24)
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