- Merck & Co. (North Wales, PA)
- …medical breakthroughs. We review the quality and reliability of clinical studies using deep scientific knowledge, statistical-analysis and high-quality data ... to support decision making in clinical trials.-The Associate Principal Scientist, Statistical Programmer supports the...and delivery of efficient, flexible, and modular analysis and reporting and submission standards that can be used for… 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
- Merck & Co. (North Wales, PA)
- … development, including: study design, placement, monitoring, analysis, regulatory reporting , and publication.Evaluating pre- clinical and translational work for ... Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our company's… more
- Novo Nordisk Inc. (Los Angeles, CA)
- …(Site Selection, Site Initiation, Monitoring, and Closure) for assigned sites and clinical trials Verifies safety reporting and the proper handling, monitoring ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...and implement Corrective and Preventive Action Plans (CAPA) Shares information , collaborates and provides relevant input and guidance to… more
- Novo Nordisk Inc. (Minneapolis, MN)
- …and community thought-leaders in an assigned territory. The Rare Renal Clinical Account Manager will be principally responsible for driving disease awareness, ... establishing NNI as a leader in the rare renal marketplace. The Rare Renal Clinical Account Manager (RRCAM) will be responsible for achieving sales targets and other… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- Director, Clinical Development Join a Legacy of Innovation 125 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of innovative ... primary source of medical accountability and oversight for one or more clinical trials Matrix management responsibilities across the internal and external network… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential 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)
- …DescriptionPosition Description: Director, Analytical R&D and Process R&D, Development Sciences & Clinical Supply Finance The Director will oversee a team of five ... for two areas:Analytical Research & Development within Development Sciences & Clinical Supply (DSCS):- organization is responsible for analytical method development… more
- 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 regulations relating to technical complaints, adverse events and other safety information in the US and Canada. Overall responsible for compliance with US… 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
- 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. (North Wales, PA)
- …of potential medical breakthroughs.Review the quality and reliability of clinical studies using deep scientific knowledge, statistical analysis and high-quality ... data to support decision making in clinical trials.Support statistical programming activities for Early Oncology clinical development projects.Responsible for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …end-to-end delivery of External data in Daiichi Sankyo R&D collaborating with Clinical and Medical teams, Functional Stakeholders, (QCP, Clinical Biomarkers, ... delivery of all 3rd party data from diverse external providers for clinical trials, companion diagnostics trials, clinical development, and regulatory… 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
- Merck & Co. (North Wales, PA)
- … clinical trial programming.Broad knowledge in developing analysis and reporting deliverables for Research & Development (R&D) projects (data, analyses, tables, ... project teams in creating SDTM deliverables for Analysis and Reporting activities and submission.Collaborating with project teams to prepare the… more
- Novo Nordisk Inc. (Shreveport, LA)
- …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
- Merck & Co. (North Wales, PA)
- …:This position provides high quality statistical programming analysis and reporting deliverables for global PK modeling and simulation stakeholders spanning ... of other team members when opportunities arise.Primary Activities :Programmatically synthesize clinical / preclinical data into analysis ready structures from varied… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and Seattle reflect the full R&D continuum, from early research through late-stage clinical development. Here, we are building for the future, creating a distinct ... of safety profile of assigned molecules/products and communicate safety information to internal and external stakeholders. Relationships This position will… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and immune disorders.Summary The Senior Director sits within Global Oncology Clinical Development, an organization dedicated to the effective strategy, design, ... execution, and interpretation of Oncology clinical trials. Position Summary / Objective Serves as a...Safety Management Team (SMT) materials- Supports overall program safety reporting (eg, Periodic Safety Update Reports (PSURs), Drug Safety… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and immune disorders. SummaryThe Senior Director sits within Global Oncology Clinical Development, an organization dedicated to the effective strategy, design, ... execution, and interpretation of Oncology clinical trials. Serves as a primary source of medical...approved Safety Management Team (SMT) materialsSupports overall program safety reporting (eg, Periodic Safety Update Reports (PSURs), Drug Safety… more
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