- System One (Rahway, NJ)
- Job Title: Associate Principal Scientist , Regulatory Affairs Location: Rahway, NJ (Hybrid) Hours/Schedule: Mon- Fri; 8am- 5pm Type: Contract Responsibilities ... The Associate Principal Scientist is responsible for developing CMC regulatory ...eligible employees health and welfare benefits coverage options, including medical , dental, vision, spending accounts, life insurance, voluntary plans,… more
- Organon & Co. (Jersey City, NJ)
- …in Organon Regulatory Chemistry, Manufacturing and Controls New Products, the Associate Principal Scientist ( Associate Director) is responsible for ... and will encompass late-stage development products and commercially approved compounds. The Associate Principal Scientist may also support project team goals and… more
- Merck (Rahway, NJ)
- **Job Description** The Associate Principal Scientist , General Medicine Publications Medical Writing, works with scientists in our company's Research Labs ... development projects and other of our Research & Development Division science. The Associate Principal Scientist is expected to collaborate with our Research &… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- We are seeking an Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, ... of study data of a clinical development program. The Associate Director leads in a matrix environment as part...to the Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Associate Director, Clinical Sciences contributes to the development, evaluation, planning and execution of hematology clinical studies and ensures scientific ... Director, Clinical Sciences Hematology, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design… more
- Pfizer (Pearl River, NY)
- …best in class medicines to patients around the world. **What You Will Achieve** As an Associate Scientist , you will be at the center of our operations and you'll ... Good Manufacturing Practices/ Good Laboratory Practice (cGMP/GLP) and all other regulatory agency requirements. + Assist in updating and writing documents associated… more
- Pfizer (Pearl River, NY)
- …class medicines to patients around the world. **What You Will Achieve** As a Senior Associate Scientist , you will be at the center of our operations and you'll ... Manufacturing Practices/ Good Laboratory Practice (cGMP/GLP) and all other regulatory agency requirements, if needed. **Qualifications** **Must-Have** + Bachelor's… more
- Pfizer (Pearl River, NY)
- …best in class medicines to patients around the world. **What You Will Achieve** As an Associate Scientist , you will be at the center of our operations and you'll ... Good Manufacturing Practices/ Good Laboratory Practice (cGMP/GLP) and all other regulatory agency requirements, if needed. + Perform other duties as assigned.… 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
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …contribute to preparations for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority) + Supports clinical/ medical data review, including ... Reports to the Senior Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise vital to design and deliver… 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
- Pfizer (Pearl River, NY)
- …Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical , prescription ... public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses… more
- Pfizer (Pearl River, NY)
- …Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical , prescription ... public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses… 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 (Pompton Plains, NJ)
- …in chemical, physical or biological science or medical laboratory technology/ medical or clinical laboratory science preferred + Associate 's degree in ... Testing program in various clinical departments, ensuring compliance with regulatory standards, and promoting patient safety. Principal Accountabilities: + Follow… 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
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …through early and/or late phase development. The Manager reports to either Associate Director or Director, Clinical Sciences and collaborates closely with Medical ... * Assists with and may authors/review documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical… 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