- Merck & Co. (Rahway, NJ)
- …Material(s):NoRequired Skills:Adaptability, Clinical Data, Clinical Operations, Clinical Study Design, Clinical Trial Compliance , ... Job DescriptionOphthalmology Clinical Scientist:Job SummaryThis position leads the scientific planning...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los… more
- Merck & Co. (North Wales, PA)
- …Material(s):n/aRequired Skills:Adaptability, Adaptability, Asset Life Cycle Management, Audits Compliance , Clinical Information Systems, Clinical ... Site Management, Clinical Testing, Clinical Trial Compliance , Communication, Detail-Oriented, Drug Regulatory Affairs, Employee Training Programs, Finance,… more
- Merck & Co. (San Diego, CA)
- …Material(s):NoRequired Skills:Adaptability, Clinical Data, Clinical Operations, Clinical Study Design, Clinical Trial Compliance , ... the operational planning and execution of one or more clinical trials or significant aspects thereof. In this position,...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance , clinical quality, technical operations or cell therapy.Experience ... floor quality oversight of the production of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom environment. This… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …working in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance , clinical quality, or cell therapy.Knowledge of cGMP and ... during the execution of regulatory inspections and audits as needed.Support compliance activities for site Quality Operations in accordance with Legend standards,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionIn partnership with the Clinical Quality Operations Lead (CQOL and Head of CQO, the CQOM is accountable for the execution of operational quality ... quality management and inspection management activities.The CQOM will oversee headquarters clinical quality operations and support clinical trial teams within… more
- Merck & Co. (Upper Gwynedd, PA)
- …--The Senior Director will report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of a supervisor, the Senior Director has ... primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our Oncology medicines span all… more
- Insmed Incorporated (San Diego, CA)
- …be responsible for the development and implementation of EDC systems to support clinical trials, ensuring data quality, compliance , and efficiency throughout the ... expertise and system documentationEnsure data integrity, system reliability, and regulatory compliance across all phases of clinical developmentTeam Leadership &… more
- Merck & Co. (Rahway, NJ)
- …Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed cardiovascular and respiratory ... the Senior Director will manage the entire cycle of clinical development, including study design, initiation, execution, monitoring, analysis, regulatory… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is part of our company's Research Laboratories and is accountable for managing the end-to-end integrated ... clinical supply chain across our company's portfolio to enable...to Settlement/Tax/Finance, Trade Operations, ISO, Relationship Management, QA, and Compliance . Primary activities include, but are not limited to:Lead… 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)
- …Scientist) has primary responsibility for the planning and directing of 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 Senior Director...applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance , clinical quality, or cell therapy.GxP Quality System knowledge, ... systems processes within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment. This role will… more
- Merck & Co. (Rahway, NJ)
- …hybridization) testing procedures, and applicable laboratory testing regulations.Experience ensuring compliance of a clinical laboratory with regulatory ... Molecular Biomarkers is responsible for translating preclinical molecular biomarkers to clinical development across all therapeutic areas and all phases of … more
- Merck & Co. (Boston, MA)
- …Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the ... area. Our company's Atherosclerosis & Metabolism medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Vice President (AVP)/Section Head, Global Clinical Development, Pediatrics will focus on driving strategy, development, and life-cycle ... stages of development therefore requiring someone who has late vaccine clinical development and lifecycle management experience.The AVP will also be responsible… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance , clinical quality, or cell therapy.Knowledge of cGMP regulations ... systems, and processes within a cell therapy manufacturing plant to support both clinical and commercial requirements in a sterile GMP environment. This role will be… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. SummaryThe Senior Director of Clinical Operations will manage clinical operations staff to ensure the ... effective and efficient execution of operational aspects of clinical study planning, implementation, data delivery and reporting. Will represent DSPD Clinical … more
- Eisai, Inc (Nutley, NJ)
- …for Good Clinical Practice (GCP) oversight, and for assuring the compliance of projects, products and programs with Eisai's Standard Operating Procedures (SOPs), ... your profile, we want to hear from you. Director, Clinical Quality Assurance The Director, Clinical Quality...you. Director, Clinical Quality Assurance The Director, Clinical Quality Assurance position is responsible for design, delivery… more
- Insmed Incorporated (San Diego, CA)
- …Quality Assurance.Full understanding of and practical experience establishing and fostering compliance with ICH E6 Guideline for Good Clinical Practice.Provide ... and Best Medium Workplaces™ lists.OverviewReporting to the Executive Director of Clinical Quality Assurance, the Director of Clinical Quality Assurance… more
