• Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …opportunity employer including veterans and people with disabilitiesSummaryThe Associate Director , Global Oncology Clinical Development (GOCD) Functional ... generation (checklist, process map, etc.), change management and detailed analysesThe Associate Director , GOCD Functional Excellence must have excellent verbal… more
    HireLifeScience (05/25/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …centered around rare diseases and immune disorders. Summary The Associate Director , Global Oncology Clinical Development (GOCD) Functional Excellence ... management and implementation planning, for GOCD non-project related initiatives. The Associate Director , GOCD Functional Excellence must have excellent verbal… more
    HireLifeScience (05/24/24)
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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 ... and collecting data to support efficacy and new product development , CMR is involved. The one thing that keeps...ready to make a difference? The Position The Assoc Director OED - Supplies, is responsible for US and… more
    HireLifeScience (05/16/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    About the Department The Clinical Development , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within ... of clinical trials is required Demonstrates technical expertise within Clinical Development , Medical Affairs, and Regulatory Affairs (CMR), staying… more
    HireLifeScience (04/26/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …aligned therapeutic / franchise area(s). Relationships Reports to the Senior Director of Value Communication and Contracting Strategy Interacts frequently in ... Essential Functions Leads pricing and contracting strategy, playbook, and guideline development for all new product launches within responsible therapeutic area,… more
    HireLifeScience (03/12/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …stud(ies).Ensures trial master file is complete and accurate for assigned stud(ies).If assigned, Associate Director , Clinical Operations may act as the Study ... regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines. The Associate Director is accountable for operational planning and… more
    HireLifeScience (05/18/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …of research and strategic partnership contracting agreements. In collaboration with the Associate Director , the Associate Manager will support CMR's ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...and external stakeholders Relationships This position reports to an Associate Director overseeing the contract management function… more
    HireLifeScience (05/22/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …an equal opportunity employer including veterans and people with disabilities.SummaryThe Associate Director will be responsible for developing and implementing ... & Simulation plans from FIH to post registration. Responsibilities include the development of Clinical Pharmacology and Modeling and Simulation plans, design… more
    HireLifeScience (04/23/24)
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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...a specific compound or indication. Responsibilities Support GMA the development of the Global Medical Affairs strategy and execution… more
    HireLifeScience (05/24/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …of clinical trial protocols. Provides medical and/or scientific direction to Clinical Operations. Represents Clinical Development on Project Teams. ... 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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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    … sub-team and to drive the development and delivery of the clinical development plan in alignment with the product development strategy.Manages ... Summary This position is responsible for providing project management, drug development expertise to Global Project Teams including strategic development more
    HireLifeScience (05/25/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …diseases and immune disorders. Job Summary: The Global Brand Associate Director is accountable for supporting the development , integration, and execution of ... provided to cross-functional teams including but not limited to product clinical development team(s), HEOR, PRA, medical affairs, manufacturing and PR. This… more
    HireLifeScience (05/20/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …in data science / business intelligence / statistics role supporting drug development and/or post marketing in clinical research, pharmaceutical, CRO or ... end-to-end delivery of AI/ML projects (from business understanding, over hands-on development to dissemination), to ensure high quality deliverables are on time… more
    HireLifeScience (05/24/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …increased complexity including post marketing projects and those involving 3rd party development . This position partners with GRLs and Clinical Safety ... may assist another Global Labeling Lead by managing labeling development or approval for either the US or EU....may assist another Global Labeling Lead by managing labeling development or approval for either the US or EU.Ensure… more
    HireLifeScience (05/22/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …- Responsible, with limited supervision, for study activities assigned, eg for a clinical study: provide input on the development of study protocol (design, ... Qualifications- At least 5 years of experience as statistician supporting drug development and/or post marketing in Clinical research, Pharmaceutical company,… more
    HireLifeScience (05/17/24)
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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 ... diverse external providers for clinical trials, companion diagnostics trials, clinical development , and regulatory submissions. This position may propose… more
    HireLifeScience (04/20/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …(CDx) in support of projects within Daiichi Sankyo's Early and Late Stage Development Portfolio. The individual will play a key role in making Precision Medicine ... Teams (GPT) for the therapeutic, covering all areas from CDx assay development through CDx approval and launchLeads CDx Partner evaluation and selection activities… more
    HireLifeScience (05/09/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …industry, vendor base, and regulatory issues for respective categories. Leads the development of sourcing strategy for respective categories. Builds and maintains a ... vendor base. Manages vendor relationships. Implement sourcing and value development roadmap and initiatives; contribute to strong supplier relationship management,… more
    HireLifeScience (05/09/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …other research areas centered around rare diseases and immune disorders. Summary The Associate Director Global Oncology Value Access & Pricing will both develop ... with global functions including but not limited to Commercial, Marketing, Medical, Clinical Development , Public & Government Affairs.Responsibilities- Lead the … more
    HireLifeScience (03/01/24)
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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, ... preparation of data for statistical analysis to obtain background rates) for development of safety documents (eg, RMP), support SMTs, SERM or other safety-related… more
    HireLifeScience (04/04/24)
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