- Merck & Co. (Rahway, NJ)
- …resolve complex data entry discrepancies and differences effectively.- Data Analysis and Reporting :-Partner with Clinical Research Managers and Clinical ... Experience: Bachelor of Science (or international equivalent) in Data Management, Management Information Systems (MIS), Biological or Clinical Sciences, or a… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …primary source of medical accountability and oversight for one or more clinical trials. Matrix management responsibilities across the internal and external network. ... medical input regarding country feasibility. Consulted on decisions related to clinical trial feasibility and contributes to the site feasibility assessment from… more
- Merck & Co. (Rahway, NJ)
- …Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our company's ... oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of clinical … more
- Merck & Co. (Rahway, NJ)
- …--The Director will report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of a supervisor, the Director has primary ... responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our Oncology medicines span all phases of… 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 ... indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and… more
- Merck & Co. (Rahway, NJ)
- …Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our company's ... oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of clinical … more
- Merck & Co. (Rahway, NJ)
- …Scientist) has primary responsibility for the planning and directing clinical research activities within the Atherosclerosis and Metabolism therapeutic area, ... - The Senior Director will manage the entire cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting… more
- Merck & Co. (Rahway, NJ)
- …Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Oncology medicines. Our ... company's Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of clinical … more
- Genmab (Plainsboro, NJ)
- …on collaboration, excellence, and a can-do attitude to achieve results.You will be reporting to Director, Global Clinical Drug Supply in Copenhagen, Denmark.Main ... to fulfilling our purpose.The Role & DepartmentGenmab is seeking an experienced Senior Clinical Drug Supply Manager to join our Global Clinical Drug Supply… more
- Insmed Incorporated (San Diego, CA)
- …Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Senior Clinical Research Scientist (CRS) will support and work predominately with the ... Clinical Trial/Indication Lead(s) and Medical Monitor(s) for assigned protocols...and study execution, from study design planning through final reporting of results Provide scientific input and review of… more
- Genmab (NJ)
- …development, data collection, data review and cleaning activities and analysis and reporting in clinical trialsExperience and understanding of GCPs, SOPs, ... Director, Data Management is operationally responsible for the oversight of Clinical Data Management activities related to the effective planning, and timely… more
- Merck & Co. (Rahway, NJ)
- …or related fields.3+ years in Project and/or Program Management supporting Information Technology, or Pharmaceutical Research or Clinical Trial Operations ... or Product Owner certificationPrior experience in the pharmaceutical industry or Clinical Trial Operations or Information Technology.Basic understanding of the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Maintains oversight of DSI contracts that are PV relevant and AE reporting language in associated contractual templates. Ensures Good Pharmacovigilance Practice and ... responsible for Call Center, individual safety case processing, and aggregate reporting for DSI products, both investigational and marketed. Maintains compliance… more
- Merck & Co. (North Wales, PA)
- …This position supports statistical programming activities for late stage drug/vaccine clinical development projects. This may include leadership of one or more ... predominantly includes the development and execution of statistical analysis and reporting deliverables (eg safety and efficacy analysis datasets, tables, listings,… more
- Novo Nordisk Inc. (Sacramento, CA)
- …Generate advocacy for Novo Nordisk products and services by sharing approved clinical and scientific information and insights Interface with key associations ... skills required (Windows, Word, Excel); prior computer experience using sales data/call reporting software ideal Mastery knowledge of the clinical management of… more
- Merck & Co. (North Wales, PA)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and ... execution of statistical analysis and reporting deliverables (eg safety and efficacy analysis datasets, tables,...listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post… more
- Merck & Co. (Rahway, NJ)
- …potential medical breakthroughs.Support statistical programming activities for Early Oncology clinical development projects.Review the quality and reliability of ... statistical analysis and high-quality data to support decision making in clinical trials.Responsible for the development and execution of statistical analysis and… more
- Novo Nordisk Inc. (Winter Park, FL)
- …Generate advocacy for Novo Nordisk products and services by sharing approved clinical and scientific information and insights Analyze and leverage understanding ... assess, create and maintain advocacy of customers aligned to company, brand and clinical goals. The OCS develops local strategies and executes local tactical plans… more
- Novo Nordisk Inc. (Milwaukee, WI)
- …Generates advocacy for Novo Nordisk products and services by sharing approved clinical and scientific information and insights with target physicians Recognizes ... skills required (Windows, Word, Excel); prior computer experience using sales data/call reporting software ideal Mastery knowledge of the clinical management of… more
- Merck & Co. (Rahway, NJ)
- …presentation skillsBroad knowledge and significant experience in developing analysis and reporting deliverables for clinical trial projects (data, analyses, ... health.This position provides high quality statistical programming analysis and reporting deliverables for global stakeholders. The Associate Principal Programmer… more
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