- 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 c ... ompany's Research & Development Division portfolio of clinical trial s .- GCS is accountable for the...packaging, and distribution- for our company development products and non -our company marketed products . - Analyzes and anticipates… more
- Merck & Co. (Rahway, NJ)
- …in root causing to identify areas for operational improvement.-Participates in critical non -pipeline activities in support of clinical supply planning group (eg, ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...a comprehensive package of benefits.- Available benefits include medical, dental , vision healthcare and other insurance benefits (for employee… more
- Merck & Co. (Rahway, NJ)
- …collection of clinical supply chain metrics and/or participate in critical non -pipeline activities as a subject matter expert in a particular area of expertise. ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...a comprehensive package of benefits.- Available benefits include medical, dental , vision healthcare and other insurance benefits (for employee… more
- Novo Nordisk Inc. (Pasco, WA)
- …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
- Merck & Co. (NJ)
- …Scientific Leaders (SLs). The role provides balanced, factual, scientific information about non -product areas of interest to the Company and replies to scientific ... with applicable policiesMaintains current knowledge and comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest (AOI) for the… more
- Merck & Co. (South San Francisco, CA)
- …ms of experienced sci e ntis ts to discover and advance the clinical development of novel therapeutic agents for cardiometabolic and ophthalmologic diseases. You ... on the discovery and development of small molecules, biologics and non -traditional therapeutics like peptides, novel biological constructs, and others. The Associate… more
- Merck & Co. (Chicago, IL)
- …Scientific Leaders (SLs). The role provides balanced, factual, scientific information about non -product areas of interest to the Company and replies to scientific ... (GMSA) strategy, including field standard operating procedures (SOPs), Good Clinical Practice (GCP) guidelines, and administrative/operational responsibilities.Location: This is… more
- Merck & Co. (North Wales, PA)
- …management; a general understanding of worldwide regulatory requirements; and with good clinical trial experience in Phase II/ III trials.- The knowledge must be ... principles and statistical methods applied to designing and analyzing clinical trials in support of worldwide regulatory submissions.This position involves… more
- Merck & Co. (Rahway, NJ)
- …and partnering for Pharmaceutical development/ CMC with Quality, Regulatory, Operations, Non - clinical , Clinical , and other functional areasExperience with ... proteins as well as the biopharmaceutic support for the oral and non -oral portfolio. Within Biologics and Biopharmaceutics, the large molecule product development… more
- Merck & Co. (Rahway, NJ)
- …programming requests in close collaboration with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data, transform the data into ... or related field plus 5-9 years SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life Sciences,… more
- Merck & Co. (Rahway, NJ)
- …Strong understanding of integration and partnering with Quality, Regulatory, Operations, Non - clinical , Clinical , and other functional areas.Demonstrated ... In summary, our team enables the translation of preclinical candidates into non -oral drug products.We are seeking a highly motivated candidate for the position… more
- Merck & Co. (Rahway, NJ)
- …the guidance of a senior-level programmer supporting early-phase oncology clinical trials. Collaborate with other programming colleagues and biostatisticians and/or ... as well as stakeholders in data management, medical writing, and clinical operations to gather and document requirements for statistical programming deliverables.… more
- Genmab (NJ)
- …Manager will support the Data Management, Statistics, Drug Safety, Medical, Clinical Pharmacology and Biomarker functions with the above by developing and ... checks of data consistenciesSupports specification and pooling of data across clinical trials within the same project.Supports in-house production of analysis… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …for overseeing the production of a personalized cell therapy to support both clinical and commercial requirements in either a Grade C or sterile cGMP environment.Key ... according to cGMP requirements.Lead a ~250+ organization responsible for either the non -sterile or sterile manufacturing processes in a 24/7 operation and be… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …be responsible for maintenance support and mechanical system operations for cGMP Clinical and Commercial Cell Therapy Manufacturing on a modified second shift ... requirements. This individual will support the organization in its build and ramp-up of clinical production and facility approval of a state of the art cell therapy… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …systems, and processes within a cell therapy manufacturing plant to support both clinical and commercial requirements in a sterile GMP environment. This role will ... the CAR-T Raritan SiteReview and approve change controls, SOPs, non -conformances, and CAPAs associated with qualification/validation execution and ensure… 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 ... risks/quality drift in external vendor and NNI processes to mitigate non -compliance and deviation occurrence Support internal and external stakeholders with issue… 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 ... risks/quality drift in external vendor and NNI processes to mitigate non -compliance and deviation occurrence Support internal and external stakeholders with issue… more
- Merck & Co. (Rahway, NJ)
- …(Analytical R&D) , PR&D (Process R&D) and PSCS (Pharmaceutical Sciences and Clinical Supply) functions.Understanding of the business workflows across the Discovery / ... a matrixed organization.- Effectively communicate to both technical and non -technical audiences.- Familiarity with IT architectural principles.Demonstrated ability to… more
- Merck & Co. (Rahway, NJ)
- …related field plus at least 2 years SAS programming experience in a clinical trial environment. Required experience and skills Must possess SAS programming skills ... have an interest and ability to work in an exploratory environment, handling non -standard data in a variety of formats with minimal requirements; and an interest… more
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