- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and members of the medical community to assist in understanding current academic, clinical trial and practice issues related to DS Oncology development and ... portfolio serve as the US Medical Affairs lead or Global lead in development committees and global medical affairs activities. Represent Medical Affairs in new… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …- Project Planning and Forecasting - Manages and is accountable for the development and control of Clinical Project Budget in support of Phase ... or US based Global Function leaders as a Finance Business Partner.Provides guidance to them during the annual and...I-III clinical studies.Partner with Project Management, Clinical Operations and other functional groups to ensure budgets… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …relationships with key stakeholders within CSPV and external functions including Clinical Development , Research Development , Regulatory Affairs. Facilitate ... areas centered around rare diseases and immune disorders. Summary Leads the development and management of DSI's local and global Strategic PV Partnerships and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …sites. These business functions include but are not limited to Clinical Operations, Clinical Development , Biostatistics and Data Management, Regulatory ... direction and serves as a knowledge source for Informatics on systems development .Responsibilities- Provide the interface between the business and the technology… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionWithin the Development Sciences and Clinical Supply (DSCS) organization, the Digital Program Manager will advance the purpose and aspiration of ... comprising of Process Research & Development , Analytical Research & Development , and Pharmaceutical Sciences & Clinical Supply. The ideal candidate… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …increased complexity including post marketing projects and those involving 3rd party development . This position partners with GRLs and Clinical Safety ... labeling in collaboration with the Global Regulatory Leads (GRLs) and Clinical Safety & Pharmacovigilance (CSPV) for assigned products. This position drives/leads… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …labeling in collaboration with the Global Regulatory Leads (GRLs) and Clinical Safety & Pharmacovigilance (CSPV) for assigned products. This position drives/leads ... the development and maintenance of the CCDS, US and EU...(HA) regulations and guidelines, internal company procedures and company business objectives. This position manages new projects and projects… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …highest level of qualityCollaborate with internal stakeholders - including IT and business resources, contracts, and procurement - to develop criteria and best ... for ensuring the design of the CSPV solution that satisfies the business process visionLead platforms and systems design and optimization to deliver best-in-class… more
- Merck & Co. (Rahway, NJ)
- …the goals, purpose and mission of our Company's Research Labs, Global Clinical Development (GCD) and GCTOPositive proven success in people management.Educational ... Job DescriptionThe Clinical Research Director (CRD) is the...responsibilities: Supports the regional GCTO leadership team, leading strategic development of their country /-cluster to deliver clinical… more
- Merck & Co. (Rahway, NJ)
- …Oncology medicines. Our Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the ... affairs, statistics, and manufacturing to manage clinical development projects; and Assist the Senior/Executive Director /AVP...with external researchers around the world; Travel on company business about twenty (20) percent of the time to… more
- Merck & Co. (Rahway, NJ)
- …- The Senior Director will manage the entire cycle of clinical development , including study design, placement, monitoring, analysis, regulatory reporting, ... and publication. - Specifically, the Senior Director may be responsible for Evaluating pre- clinical ...and translational work for the purpose of generating early clinical development plan and Investigational new drug… more
- Genmab (Plainsboro, NJ)
- …authentic is essential to fulfilling our purpose.The RoleGenmab is searching for an experienced Director , Global Clinical Drug Supply to be part of Global ... people who are caring, candid, and impact-driven to our business , which is innovative and rooted in science, we...bringing medicines to cancer patients and other serious diseases. Director , Global Clinical Drug Supply will work… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …of technical training across all CMR functions, and compliance across clinical development , medical, and regulatory roles/processes/SOPs Develop and implement ... will provide valuable support and consultation to Senior Leaders in the Line of Business . In this role, the Director will demonstrate exceptional ability to… more
- Merck & Co. (Rahway, NJ)
- …Global Clinical Supply (GCS) organization, within our Research & Development (R&D) Division , is accountable for managing the 'end-to-end' integrated ... consultation or operations support needsEnsure an exquisite partnership with Global Clinical Trial Operations, Regulatory and other Development Sciences and… more
- Merck & Co. (Rahway, NJ)
- …Global Clinical Supply (GCS) organization, within our Research & Development (R&D) Division , is accountable for managing the 'end-to-end' integrated ... clinical supply chain across all of the R&D portfolio...Activities include, but are not limited to: Talent attraction, development and retentionPerformance managementEnsures Efficient and compliant inventory management… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … informatics tools Drives the development and delivery of innovative clinical informatics solutions and services response to business requirements and ... you ready to make a difference? The Position The Director , Clinical Informatics in the Clinical...Clinical Data Science & Evidence (CDSE) department develops clinical and medical informatics software and system development… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … Clinical Data Science & Evidence (CDSE) department of NNI focused on clinical informatics tools development to support the CMR organization. This individual ... will serve as a subject matter expect on clinical and medical informatics software and system development...measurements that are consistent with the priorities of the business , and that interim reviews are held so that… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …to support optimization of access & reimbursement, clinical practice, product development and registration. The Director serves as a visible PED champion ... method review) Facilitates integration of the US PED strategy into clinical development programs, post-authorization and commercial research activities and… more
- Merck & Co. (Rahway, NJ)
- … clinical development teams and the operational/executional arms within the business . The Program Clinical Supplies Project Manager serves as the primary ... development process & connectivity between functions supporting pipeline (ie clinical development , Compound Management Coordination , supply chain, & human… more
- Genmab (Plainsboro, NJ)
- …serious diseases. From our people who are caring, candid, and impact-driven to our business , which is innovative and rooted in science, we believe that being proudly ... our best, and authentic is essential to fulfilling our purpose.The RoleThe Global Clinical Trial Manager (GCTM) is accountable for the end-to-end delivery of a… more
