- Merck & Co. (North Wales, PA)
- …drugs, vaccines 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 ethical standards.The Senior Director ( Senior Principal Scientist) has primary...based on these clinical development strategiesMonitoring and managing the conduct of ongoing or new clinical trials for investigational… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … within the pharmaceutical or biotechnology industry. Relationship This job reports to the Senior Director of the GxP Compliance & Technical Operations or the ... consistency and compliance with FDA, EMA, and other regulatory guidelines Conduct regular audits of GxP documentation to verify compliance and identify… more
- Merck & Co. (MA)
- Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the strategic planning and directing clinical research activities ... investigational compounds in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of clinical development,… more
- Merck & Co. (Boston, MA)
- Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or ... span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage clinical development… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …training delivery in a highly regulated environment. Relationship This job reports to the Senior Director of the GxP Compliance & Technical Operations or the GxP ... deliver comprehensive training programs that support clinical excellence, regulatory compliance , and medical affairs expertise across our global CMR organization.… more
- Insmed Incorporated (San Diego, CA)
- …of science, we're in. Are you?About the Role:Insmed is seeking a Senior Research Associate - Lab Technician with specialized expertise in supporting preclinical ... biospecimens, including processing, storage, and preparation for downstream multi-omics analyses. Conduct laboratory assays related to vector biodistribution, transgene expression,… more
- Tris Pharma (Monmouth Junction, NJ)
- …Director/Director, Procurement. Title and salary commensurate with experience. The Director/ Senior Director, Procurement is responsible for multiple facets of the ... supplier relationship management, procurement systems functionality/workflows and assurance of compliance with GxP and other company and regulatory agency… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Senior Medical Affairs Administrative Assistant will support Medical Affairs Field Medical, Strategy & ... will provide administrative support and coordination to the department and conduct contracting, invoicing and data entry to support department's projects. Essential… more
- Eisai, Inc (Nutley, NJ)
- …is responsible for Good Clinical Practice (GCP) and for assuring the compliance of projects, products and programs with Eisai's Standard Operating Procedures (SOPs), ... inspection management, issue management, and oversight of the quality management system). Conduct complex audits of sites, vendors and internal process.Train junior… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …capabilities through strategic vendor partnerships. Relationship This job reports to the Senior Director of the GxP Compliance & Technical Operations. This ... Strategy & Development Develop a holistic learning strategy focused on enhancing employee knowledge and compliance within the CMR organization Design and… more
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