- Merck & Co. (Rahway, NJ)
- …(GCP) studies, and occasionally Good Laboratory Practice (GLP) studies.The Associate Principal Scientist is the primary clinical study team leader and has ... Job DescriptionJOB DESCRIPTION SUMMARYThe Associate Principal Scientist is a DVM/VMD and/or PhD whose primary...primary function is to design, coordinate, monitor, and report clinical laboratory and field studies that will support the… more
- Merck & Co. (Rahway, NJ)
- …and existing products to produce safe, effective, innovative medicine. -The Early Clinical Scientist /ECS coordinates the design, planning and execution of early ... in global healthcare. - -Translational Medicine is responsible for early clinical development of novel therapeutics, working in close collaboration with Discovery… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Clinical Development teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs 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… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Director (Principal Scientist ) has primary responsibility for the planning and directing of clinical research activities involving new or ... marketed Oncology medicines. Our company Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Director (Principal Scientist ) has primary responsibility for the planning and directing 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 Director will manage… 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
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing applications/supplements ... laboratory members, the Contract Manufacturing Organization (CMO), Labeling members and Clinical members. This position works with non-standard problems of some… more
- Merck & Co. (Rahway, NJ)
- …science of preclinical discovery into compounds ready for assessment in large clinical populations.We are seeking a highly qualified physician- scientist with a ... Job Description Senior Principal Scientist Translational Medicine, Immunology Translational Medicine in our...experience in the pharmaceutical industry and Immunology R&D and clinical and academic expertise in Immunology-related areas such as… more
- Merck & Co. (Rahway, NJ)
- …for world-wide regulatory application submissions of drug and vaccine clinical development projects. Accountability predominantly includes submission data standards ... and keeping current with industry submission data standards including SDTM, ADaM, clinical site data for CDER inspection planning, etc.The incumbent will be… more
- Merck & Co. (Rahway, NJ)
- Job Description BPR&D Downstream Principal Scientist Job Description: - - Our Scientists are our Inventors. Using innovative thinking, state-of-the-art facilities, ... bioprocessing to join Biologics Process Research & Development (BPR&D) as a Principal Scientist .- - BPR&D within our company's Research Lab oratories is on a mission… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPrincipal Scientist - Mixed Modalities, Sterile Product DevelopmentThe Mixed Modalities team within Sterile Product Development is responsible for ... products.We are seeking a highly motivated candidate for the position of Principal Scientist (R5) focused on developing parenteral drug products across a range of… more
- Merck & Co. (Rahway, NJ)
- …& Development team that designs and develops benchtop/low-volume to high-volume clinical and commercial assembly equipment and processes for medical devices/drug ... using semi-automated and automated equipment, conduct functional testing, assist in clinical batch manufacture as an equipment subject matter expert, assist with… 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
- 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 ... including data steps, procedures, SAS/MACRO, SAS/GRAPH.Knowledge and skills in developing analysis and reporting deliverables for R&D projects (data, analyses, tables, graphics, listings); knowledge of pharmaceutical development processes; and knowledge in… more
- Merck & Co. (Rahway, NJ)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and ... 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)
- Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving new ... 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. (Rahway, NJ)
- …We are seeking an experienced and skilled Cheminformatician and AI/ML data scientist to join the Cheminformatics group within Modeling and Informatics (M&I) at ... that accelerate the decision-making process from hit identification to clinical candidate delivery across different therapeutic areas and modalities at… more
- Merck & Co. (Rahway, NJ)
- …product release testing across the entirety of our non-sterile and sterile clinical portfolio. The Director is responsible for ensuring cGMP compliance and ... budget management as necessary.Primary Responsibilities:Leading a team of specialists and scientist supporting raw material release and medical device & combination… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …Associate Director a typical day may include the following: + May function as lead Clinical Scientist for program, and/or as delegate of Therapeutic area Lead ... Clinical Scientist + Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may… more
- Bausch Health (Bridgewater, NJ)
- …creates itwhere your skills and values drive our collective progress and impact. The Clinical Scientist will play a critical role in the design, execution, and ... reporting of clinical studies, with a strong focus on regulatory submissions,...New Drug Applications (NDAs). This position requires expertise in clinical trial data analysis, protocol development, and regulatory documentation,… more
