- Eclaro (Middlesex, NJ)
- …rewarding opportunity! Position Overview: We are seeking a highly motivated and detail-oriented US Medical Scientist Associate to join our medical ... Scientist Associate Job Number: 24-03333 Be... Scientist Associate Job Number: 24-03333 Be part of a...play a critical role in executing the targeted therapies medical strategy including promotional review. This position requires a… more
- Merck (Rahway, NJ)
- **Job Description** The Associate Principal Scientist of Device Technology Assessment and Early Development will spearhead early-stage device technology ... medical device and/or combination product space. + In-depth knowledge of medical device development, regulatory requirements, and quality standards, with a… more
- Merck (Rahway, NJ)
- …their knowledge of product and process development in the (bio)pharmaceutical and/or medical device industries to set tactical and strategic direction on programs ... ensure products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements. This position will lead… more
- Merck (Rahway, NJ)
- …state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. The incumbent is responsible for… more
- City of New York (New York, NY)
- …evaluating data to measure inspection results. Supervising and leading a team of Scientist Water Ecologists II, Scientist Water Ecologists I, and Scientist ... operation records, drawings and specifications of water treatment systems to establish regulatory compliance. Serving as a primary customer service liaison for the… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. Drafts development plans,… more
- Merck (Rahway, NJ)
- …a cross-functional Senior/ Executive Director group of experts in commercialization, regulatory affairs, statistics, medical affairs and manufacturing to manage ... 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… more
- Atlantic Health System (Summit, NJ)
- …in chemical, physical or biological science or medical laboratory technology/ medical or clinical laboratory science preferred + Associate 's degree in ... revision of procedures and documentation related to accreditation, adhering to all regulatory requirements for various authorities, including but not limited to CAP,… more
- Atlantic Health System (Morristown, NJ)
- …in chemical, physical or biological science or medical laboratory technology/ medical or clinical laboratory science preferred + Associate 's degree in ... revision of procedures and documentation related to accreditation, adhering to all regulatory requirements for various authorities, including but not limited to CAP,… more
- New York Genome Center (New York, NY)
- …are looking for a motivated individual to work as a Postdoctoral Research Associate within a highly creative and dynamic research team of scientists, computational ... We are interested in developing computational and experimental tools to map the regulatory wiring of the chromatin to interrogate the regulatory variation… more
- New York Genome Center (New York, NY)
- …locally and internationally. About the Position We are looking for a postdoctoral scientist eager to understand the impact of human genetic variation on gene ... the postdoc, but possible projects include developmental GTEx (https://dgtex.org/) , regulatory variant mapping and characterization large single-cell data from T… more
- Bristol Myers Squibb (Berkeley Heights, NJ)
- …Lead, the GBS Planning and Execution Lead, statistical programmers, external partners, medical monitor, protocol manager, data manager, PK scientist , and other ... treatment we pioneer. Join us and make a difference. **Purpose** The Associate Director, Biostatistics is a core member of cross-functional development teams and… more
- Bristol Myers Squibb (Princeton, NJ)
- …Lead, the GBS Planning and Execution Lead, statistical programmers, external partners, medical monitor, protocol manager, data manager, PK scientist , and other ... their personal lives. Read more: careers.bms.com/working-with-us . **Purpose** The Associate Director, Biostatistics is a core member of cross-functional development… more
- Novo Nordisk (Plainsboro, NJ)
- …Surveillance, US East Coast Development Hub. Key internal stakeholders include Medical & Science, Clinical Operations, Regulatory Affairs, Data Management, ... of Senior Global Safety Lead(s), Global Safety Lead(s) and Global Safety Scientist (s)/ Associate within Safety Surveillance. Essential Functions + Innovation and… more
