- Merck & Co. (Rahway, NJ)
- …function is to design, coordinate, monitor, and report clinical laboratory and field studies that will support the regulatory approval of new companion animal and ... candidate be responsible for the conduct of Good Clinical Practice (GCP) studies , and occasionally Good Laboratory Practice (GLP) studies .The Associate Principal… more
- Merck & Co. (South San Francisco, CA)
- …cross-functional teams that provide line-of-sight from First-in-Human studies through clinical-Proof-of-Concept. This-includes Experimental Medicine studies ... into the earliest stages of target identification and validation, and executing clinical studies to evaluate the relevance of potential targets to human disease in… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …centered around rare diseases and immune disorders. Summary Position leads complex studies in study design, statistical analysis and interpretation of results with ... and clinical study report (CSR): Leads statistical activities for complex studies including study design, protocol development, CRF review, SAP development, analysis… more
- Legend Biotech USA, Inc. (Piscataway, NJ)
- …to join our in vivo pharmacology team responsible for conducting in vivo studies with mice and NHP to support pipeline development. This position will report ... extensive knowledge and hands-on experience in conducting in vivo Pharmacology studies , especially in conducting cell-therapy based studies . The candidate… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Clinical Development teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs and new ... for investigational or marketed agents.Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new… more
- Merck & Co. (Rahway, NJ)
- …policymakers, HTA/reimbursement agencies, and health systems globally.Types of studies executed include prospective and retrospective observational studies ... programsIn collaboration with internal teams and external partners, designs studies , authors study protocols, develops measurement questionnaires, case report forms,… more
- Merck & Co. (Rahway, NJ)
- …Director may be responsible for: -Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug ... Supervise the activities of Clinical Scientists in the execution of clinical studies . --Work closely with a cross-functional group of experts in commercialization,… more
- Merck & Co. (Rahway, NJ)
- …To inform and contribute to the value evidence plan and associated studies which demonstrate clinical, economic, and patient-centered value. The work will support ... assets for cancer treatment.To design and execute observational and real-world studies , designed to demonstrate value in support of HTA, reimbursement, provider,… more
- Merck & Co. (Rahway, NJ)
- …clinical trials for investigational drugsAnalyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as ... the activities of Clinical Scientists in the execution of clinical studies .Work closely with a cross-functional group of experts in commercialization, regulatory… more
- Merck & Co. (NC)
- …approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies . The Regional Medical Scientific Director serves as a ... our AOI to determine the alignment with our research strategies, studies concepts,-scientific merit, and qualifications for a specific compound or trial.Enhances… more
- Merck & Co. (San Diego, CA)
- …work in a matrixed environment with a focus on preclinical IND-enabling studies , and translational studies enabling indication prioritization and rationale ... to support target validation, antibody drug screening, mechanism of action studies , biomarker identification in the preclinical and IND-enabling spaceDeveloping and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …in Oncology including advisory boards, Congress activities, and investigator initiated studies , advocacy and sponsorships. Interact with investigators and members of ... publication/ public disclosure and interpretation of scientific data generated by studies conducted by the Oncology teams. Oversee the development of scientific… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …programs concurrently. This position will manage coding resources of assigned studies . This position requires a strong working knowledge of medical terminology ... programs meeting quality and time expectations for both in-house and outsourced studies . Provides medical coding expertise and guidance to the program teams… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …across the internal and external network. Manages Phase 1-3 studies (depending on assignment) with demonstrated decision-making capabilitiesProvides medical and ... scientific expertise to cross-functional DSI colleagues.Responsibilities: Medical Monitoring:For studies in which Medical Monitoring activities are conducted in-house:Provides… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …and/or review manufacturing process transfer plans, protocols, and reports.Design studies , draft protocol, oversee execution and draft reports necessary to ... platforms for cell therapy development and manufacturing.Perform technical feasibility studies related to process improvement and implementation of new manufacturing… more
- Merck & Co. (Rahway, NJ)
- …investigational or marketed Oncology drugs.Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as ... in ensuring that appropriate corporate personnel are informed of the progress of studies of our company's and competitors' drugs and internal and external expert… more
- Merck & Co. (Rahway, NJ)
- …for investigational or marketed drugs Analyzing and summarizing clinical findings from studies to support decisions regarding safety and efficacy as well as new ... Supervise the activities of Clinical Scientists in the execution of clinical studies Work closely with a cross-functional group of experts in commercialization,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for a smooth consolidation process. Also responsible for managing various studies including late-stage budget and forecasting, analysis, strategic planning, internal ... Clinical Project Budget templates in support of early phase to late-stage clinical studies . Accountable for the control and reporting of GEMRAD approved budgets. On… more
- Merck & Co. (Rahway, NJ)
- …plans for all clinical supply activities associated with the clinical studies in their assigned compound(s)/ program(s). The incumbent must have demonstrated ... and ensures proper allocation of drug product as needed across studies within assigned program(s).-Responsible for identifying significant supply risks associated… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …negotiations through understanding and tactics to develop, execute and deliver clinical studies /programs on time with a focus on budget, compliance and quality. ... research partnerships and other collaboration agreements sponsorships, Investigator Sponsored Studies (ISS) and supplier service agreements Ensures compliance with… more
