- Merck & Co. (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
- Merck & Co. (Rahway, NJ)
- …department of our Research & Development Division is seeking applicants for an Associate Principal Scientist position available at its Kenilworth, New Jersey ... research facility.- The Associate Principal Scientist is a laboratory-based scientific role tasked with solving complex analytical problems at the interface of… 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
- Merck (Rahway, NJ)
- **Job Description** ** Associate Principal Scientist , Biologics Analytical Research & Development** Our Research Scientists are our Inventors. We identify and ... department of our Research & Development Division is seeking applicants for an Associate Principal Scientist position available at its Kenilworth, New Jersey… 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
- Pfizer (New York, NY)
- …and consistency of clinical data. Your work will bridge evidence-based medical decision support with colleagues and stakeholders, enhancing health and treatment ... ensuring accurate, timely, and consistent clinical data reaches the medical department and other groups. + Develop data management...a leadership role, and serve as a Clinical Data Scientist and Trial Lead for clinical trials. + Act… 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
