- 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 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
- Merck & Co. (Rahway, NJ)
- …of our Research & Development Division is seeking applicants for a Senior Scientist position available at its Rahway, New Jersey research facility. The Senior ... Scientist is a laboratory-based scientific role tasked with solving...of methods for release, characterization, and stability testing of clinical trial material and in support of product and… more
- Merck & Co. (Rahway, NJ)
- …SummaryUnder the guidance of a senior leader, a Principal Scientist /Director, has primary responsibility for developing value evidence strategies, and ... resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses,… more
- Merck & Co. (Rahway, NJ)
- …Enabling Technologies Department in Rahway, New Jersey is seeking a Senior Scientist to expand our capabilities to design and engineer proteins with novel ... the development of novel proteins to produce therapeutics to support both clinical and commercial manufacturing. The candidate will work closely with a diverse… 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)
- …Health is seeking a motivated individual to work as a bioanalytical bench scientist within its Good Laboratory Practices (GLP) bioanalytical laboratory. This is a ... bioanalytical scientist position with primary duties in preparing and analyzing...plasma and other biological samples to support pharmacokinetic, toxicokinetic, clinical efficacy and/or human food safety studies in a… 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)
- …barriers to reimbursement and market access, and provide input into clinical , regulatory, payer/access, marketing and evidence generation strategies and programs.In ... Pharmacy (AMCP) dossiers for US payers, and Global Value Dossiers.Develop supplementary clinical data package in close partnership with markets and HTA statistics… more
- Merck & Co. (Rahway, NJ)
- …other team members when opportunities arise. Primary Activities :Programmatically synthesize clinical / preclinical data into analysis ready structures from varied ... or related field plus 9 years SAS programming experience in a clinical trial environmentMS in Computer Science, Statistics, Applied Mathematics, Life Sciences,… 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)
- …on our discovery organization, from target identification through delivery of clinical candidates across our fast-growing peptide project portfolio. With in-house ... access to the most innovative screening techniques, and world-class medicinal chemistry, this position offers a wealth of opportunities to impact our discovery pipeline and ultimately save and improve patient lives.- Key responsibilities will include:… more
- Eisai, Inc (Nutley, NJ)
- …Operations Group at Eisai, Inc. is looking for Associate Director - Data Scientist /Programmer to create insightful AI powered instantaneous dashboards . The Data ... Scientist will work closely with Data Operations and Biostatisticians...and development processes.Comprehensive Data Integration: Integrate diverse data sources ( clinical , biological, etc.) to create comprehensive analyses that provide… 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
