• Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …and Modeling and Simulation plans, design and lead study teams to execute Clinical Pharmacology studies , conduct hands on population PK and PKPD analyses and ... an equal opportunity employer including veterans and people with disabilities.SummaryThe Associate Director will be responsible for developing and implementing… more
    HireLifeScience (04/23/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …biomarker strategy in collaboration with Translational Medicine/Clin Pharm; May act as Clinical study leader (CSL) Study Planning and Execution: Provides ... trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs.… more
    HireLifeScience (04/18/24)
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  • Merck & Co. (Rahway, NJ)
    …Description: Global Clinical Data Standards Therapeutic Area Lead The Associate Director , Global Clinical Data Standards Therapeutic Area ... clinical data standards development.Advanced knowledge and leading-edge skills in clinical data standards. Study Data Tabulation Model (SDTM) expertise.InForm… more
    HireLifeScience (05/10/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …role is primarily a tactical study delivery role, reporting into an Associate Director (or above) responsible for Operational Study Strategy. This ... will be responsible for ensuring the delivery execution of clinical studies in one or more geographic... trial performance and quality metrics and share with study team, Operations Program Lead, and Sr. Director more
    HireLifeScience (05/09/24)
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  • Merck & Co. (Rahway, NJ)
    …the Quantitative Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams… more
    HireLifeScience (05/10/24)
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  • Merck & Co. (Rahway, NJ)
    …engine that drives our Company's biopharmaceutical business.Under the guidance of the Director , Pharmaceutical Sciences and Clinical Supply (PSCS), this position ... Job DescriptionAssociate Director , Financial Planning & Analysis, Drug Supply (GCS)Our...( drive break-through science through drug discovery, development and clinical evaluation to address significant unmet medical need.- Finance… more
    HireLifeScience (05/09/24)
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  • Merck & Co. (Rahway, NJ)
    …ensure strong monitoring in our clinical trials. Under the oversight of the Clinical Research Director (CRD) or Head of Site Management and Monitoring, the ... of 6-14 Clinical Research Associates (CRAs) and to ensure excellent study and site performance with strict adherence to local regulations, company Standard… more
    HireLifeScience (05/11/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …outsourced or contracted activities utilizing both performance and quality measurements.The Associate Director , SCBM Financial Reporting & Strategy position ... management and liaises with internal/external stakeholders on cross-functional initiatives.The Associate Director , SCBM Financial Reporting & Strategy's… more
    HireLifeScience (05/10/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …research areas centered around rare diseases and immune disorders. Summary The Associate Director Global Medical Affairs Oncology (GMA), under the direction ... of the Senior Director , GMA Oncology (Global Medical Affairs team lead for...as medical lead for select company-sponsored GMA evidence generating studies /projects. Manages all medical aspects such as study more
    HireLifeScience (04/30/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …relevant regulatory requirements. This position has experience working on Phase I-IV study studies within the medical device and/or pharmaceutical industry ... according to applicable Daiichi Sankyo and regulatory requirements.Functional Expertise:Reviews/approves clinical study related documents that are owned by… more
    HireLifeScience (03/16/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …equal opportunity employer including veterans and people with disabilities. Summary The Associate Director , External Data Management, is accountable for the ... end-to-end delivery of External data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance, CROs and… more
    HireLifeScience (04/20/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …areas centered around rare diseases and immune disorders. Summary The CRA Oversight Associate Director plays an integral role in the strategic development, ... capacity management in accordance with budgetary requirements and emerging priorities to ensure studies are delivered as planned and critical study timelines are… more
    HireLifeScience (03/15/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …vendor selection criteria.- Problem solves and negotiates in most service types, studies , and programs- Responsible for the development and management of other ad ... preferred Experience- 7 or More Years Outsourcing, health sciences or related field ( clinical trials) required- 7 or More Years Deep experience in pharma procurement… more
    HireLifeScience (05/09/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …review), Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex ... disabilities.SummaryThis position supports early phase oncology development and leads complex studies in study design, statistical analysis and interpretation of… more
    HireLifeScience (04/04/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …areas centered around rare diseases and immune disorders. SUMMARYThe Associate Director , Pharmacoepidemiology position provides epidemiologic, methodological, ... or independently leads the design, preparation and analysis of epidemiologic studies , including real-word evidence (RWE), supporting senior management in various… more
    HireLifeScience (04/04/24)
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  • Legend Biotech USA, Inc. (Piscataway, NJ)
    …immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking an Associate Director Immuno-Oncology as part of the Research and Development team ... cell-based therapies. We are seeking an experienced and dynamic Associate Director to lead our in vivo...to drive the successful translation of preclinical findings into clinical applications. Your expertise will be critical in advancing… more
    HireLifeScience (05/04/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …research areas centered around rare diseases and immune disorders. Summary The Associate Director , Quantitative Systems Pharmacology (QSP) will work within the ... into systems (disease) modelsContribute to the design, execution and interpretation of clinical and non- clinical studies .Partner with external groups to… more
    HireLifeScience (04/23/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …and control of Clinical Project Budget in support of Phase I-III clinical studies . Partner with Project Management, Clinical Operations and other ... global business partners to develop budgets and analytics for ongoing and new pipeline studies in support of the annual process of extracting the optimal value out… more
    HireLifeScience (04/23/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …guiding other internal programmer or by self, perform programmatic review of Study Date Tabulation Model (SDTM) and analysis (including Analysis Data Model (ADaM)) ... ensure analysis dataset in compliance with CDISC and submission requirement, review study submission data package and ensure its quality and integrity.- Provide… more
    HireLifeScience (04/03/24)
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  • Merck & Co. (Rahway, NJ)
    …effective, innovative medicine.The Global Clinical Data Standards Vocabulary Specialist, Associate Director , is a subject matter expert in CDISC Controlled ... standards development teamsThe Vocabulary Specialist maintains knowledge of new technologies, clinical study data standards, regulatory requirements emerging in… more
    HireLifeScience (04/19/24)
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