- Novo Nordisk Inc. (Plainsboro, NJ)
- …you ready to make a difference? The Position Reporting to the head of Clinical , medical, Regulatory (CMR) Business Operations, the Associate Director (AD) is ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...find better and more innovative ways to improve their quality of life. We're changing lives for a living.… 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 ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Merck & Co. (Rahway, NJ)
- …benefit of patients and global human health.This position provides high quality statistical programming analysis and reporting deliverables for global stakeholders. ... programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data into… more
- Novo Nordisk Inc. (Anchorage, AK)
- …assess, create and maintain advocacy of customers aligned to company, brand and clinical goals. The OCS develops local strategies and executes local tactical plans ... partners. The OCS also assists their customers with their local clinical and educational initiatives by coordinating company resources (eg, counterparts, materials,… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …A minimum of 1 year of leadership experience is also required.Experience in clinical quality , method development, cell banking, cell therapy, or Research & ... working with Quality systems is required.Experience with quality support in clinical /commercial manufacture or NPI...skills are required.This position may require occasional travel to partner sites in NJ as business demands.Candidates… more
- Merck & Co. (North Wales, PA)
- …to engage key stakeholders.Demonstrated success in the assurance of deliverable quality and process compliance.Familiarity with statistics and clinical data ... 9 years Statistical Analysis System (SAS) programming experience in a clinical trial environment.MS (preferred) in Computer Science, Statistics, Applied Mathematics,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and cross- regional representatives on the labeling review teams as well as with business partners to achieve high quality and accurate labeling in support of ... labeling in collaboration with the Global Regulatory Leads (GRLs) and Clinical Safety & Pharmacovigilance (CSPV) for assigned products. This position drives/leads… more
- Merck & Co. (Rahway, NJ)
- …of analytical methodologies to characterize and release raw materials, package components, clinical drug substance, and clinical drug product for our small ... Excellence. The role also involves strategic partnering with Development Quality , Process Research & Development, Pharmaceutical Operations, and other parts… more
- Merck & Co. (North Wales, PA)
- Job DescriptionResponsibilities :This position provides high quality statistical programming analysis and reporting deliverables for global PK modeling and ... of other team members when opportunities arise.Primary Activities :Programmatically synthesize clinical / preclinical data into analysis ready structures from varied… more
- Merck & Co. (Rahway, NJ)
- …solid understanding of integration and partnering for Pharmaceutical development/ CMC with Quality , Regulatory, Operations, Non- clinical , Clinical , and other ... stakeholders across organizations such as Regulatory CMC, formulation functions, and clinical functions to ensure timebound progression of portfolio, initiatives for… more
