- Merck & Co. (Rahway, NJ)
- …Molecular Biomarkers (TMB) is responsible for translating preclinical molecular biomarkers to clinical development across all therapeutic areas and all phases of ... clinical development at our Company's Research laboratories. TMB laboratories...confirm engagement of therapeutic targets and understand mechanisms of drug action and patient response.Position Overview: The Flow Cytometry… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full our ... Research & Development Division portfolio of clinical trial s .- GCS is accountable for the...the timelines for bulk manufacturing needs and release of drug product across assigned program(s) . - Works directly… more
- Genmab (Plainsboro, NJ)
- …for trials managed by direct reports.Comprehensive knowledge of trial execution and clinical drug development.In-depth understanding of Good Clinical ... best, and authentic is essential to fulfilling our purpose.Overview The Global Clinical Trial Manager, Team Manager (GCTM-TM) is responsible for line management of… more
- Merck & Co. (Rahway, NJ)
- …the role of Associate Director QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to ... pharmacology and pharmacometrics of oncology drugs from post-PCC to registration. Associate Directors are emerging leaders in the field of quantitative drug… more
- Merck & Co. (Rahway, NJ)
- …on drug /vaccine development programs, and author or co-author strategic documents. Associate Directors are expected to have or be developing expertise in several ... clinical trial design and Go/No Go decisionsFraming critical drug development questions for optimizing model-informed development-Responsible for developing and… more
- Merck & Co. (Rahway, NJ)
- …clinical and translational work for the purpose of generating early clinical development plan and Investigational New Drug applications.-Developing ... to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publications.Participation in internal and… more
- Merck & Co. (Rahway, NJ)
- …pathophysiology in Cardiovascular & Respiratory. Demonstrate a strong track record in early clinical drug development, including the principles of clinical ... Job DescriptionThe Associate Vice President (AVP) will be responsible for...strategy, bridging the continuum from Discovery Research through Late-Stage Clinical Development.- The AVP provides strategic oversight for the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Job Summary: The incumbent will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in adherence to Good ... Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food...Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International Conference on… more
- Merck & Co. (North Wales, PA)
- …supports statistical programming activities for multiple and/or late stage drug /vaccine clinical development projects. -Accountability predominantly includes the ... 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)
- …stakeholders, and successfully execute, design verification strategies for assigned drug -device combination product program(s) for successful clinical ... which focuses on the design, development, and commercialization of novel biologic/ drug /vaccine-device combination products for safe and effective delivery to their… more
- Merck & Co. (Rahway, NJ)
- …position of Associate Principal Scientist (R4) focused on developing parenteral drug products across a range of modalities that can include small molecules, ... process selection. In summary, our team enables the translation of preclinical candidates into non-oral drug products. Our team is looking for a candidate for the… more
- Merck & Co. (Rahway, NJ)
- …Analytical Research and Development (SMAR&D) group has an exciting opportunity for an Associate Principal Scientist based in Rahway, NJ. Join us and experience our ... science and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global… more
- Genmab (Plainsboro, NJ)
- …our best, and authentic is essential to fulfilling our purpose.The Role The Associate Director of US Medical Affairs Hematology Strategy will report to the Director, ... market through collaboration with US Commercialization, Global Medical Affairs, Clinical Development, Regulatory, and other cross functional teams.We have a… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- Legend Biotech is seeking a Warehouse Operations Associate as part of the Warehouse & Logistics team based in Raritan, NJ. Role OverviewThe Warehouse Operations ... Associate will be part of the Technical Operations Supply...production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment.… more
- Merck & Co. (Rahway, NJ)
- …within our company's Research Laboratories is responsible for developing the drug substance manufacturing processes for our company's biologics pipeline. We work ... closely with colleagues in Discovery, Pre- clinical and Early Development to rapidly develop manufacturing processes...our Downstream Process Development and Engineering group as an Associate Principal Scientist.- In this role, you will work… more
- Merck & Co. (Rahway, NJ)
- …Dialog, etc.)Familiarity with small molecules, biologics, and vaccinesBroad understanding of drug discovery, development and research, clinical data coding and ... Job DescriptionThe Associate Director of Scientific Nomenclature and Reference Data...and CAS standards and rulesReference DataUtilizing knowledge of the drug development process and of master data principles for… more
- Merck & Co. (Rahway, NJ)
- …manufacturing enzyme processes that meet target yield, activity, and purity to ensure clinical and commercial drug substance needs. This individual will play a ... to support manufacturing of enzymatic catalysts for small molecule drug substance applications.- Through direct, lab-based contributions and scientific supervision… 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 ... The Position We are seeking a dynamic and experienced Regulatory Affairs Labeling Associate Manager to oversee and lead critical tasks related to final printed… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …with some supervision. This position contributes to specific aspects of drug development plans with minimal supervision and contributes to documents submitted ... Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies… more
- Merck & Co. (Rahway, NJ)
- …validation of Mass Spectrometry based assays that are deployed in support of clinical trials. The candidate for this Associate Principal Scientist position ... Molecular Biomarkers (TMB) is responsible for the development and execution of clinical biomarker assays across all therapeutic areas and all phases of … more
