- J&J Family of Companies (Horsham, PA)
- …States of America, Titusville, New Jersey, United States of America **Job Description:** The Principal Scientist , Safety Data Science leads the ... development and deployment of medical safety data models into production. This role plays a pivotal part in advancing AI/Machine Learning (ML) capabilities… more
- J&J Family of Companies (Spring House, PA)
- …Sciences and Translational Safety (PSTS), is seeking a highly motivated Senior Principal Scientist to lead the delivery of transformative data analytics ... **We are searching for the best talent for a Senior Principal Scientist , Computational Pathobiologist to be located in Spring… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …all relevant safety protocols and guidelines. **Education & Experience:** + Principal Scientist Level: Ph.D. in physical chemistry, biophysics, materials or ... using novel applications of solid-state characterization techniques. **Position Overview:** As a Principal Scientist in the AMC group, you will be responsible… more
- CUNY (New York, NY)
- Principal Research Scientist /Research Associate - Magnetic Resonance Imaging - CUNY Advanced Science Research Center **GENERAL DUTIES** Conducts academic ... Center enhances New York City's intellectual and cultural life. ASRC seeks a Principal Research Scientist /Research Associate to join the ASRC's MRI facility.… more
- Merck (West Point, PA)
- **Job Description** ** Principal Scientist (R5), Clinical Pathology, Pathology, Non-clinical Drug Safety , West Point** Our company is a leading global ... and infectious diseases as well as cancer. **About Us:** The Nonclinical Drug Safety organization at our Research Laboratories in West Point, Pennsylvania is seeking… more
- Amazon (New York, NY)
- …logistics through advanced AI and foundation models. We are seeking an exceptional Principal Applied Scientist to help develop innovative foundation models that ... solutions for dynamic real-world environments. Your team will leverage Amazon's vast data and computational resources to tackle ambitious problems across a diverse… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …agency requirements and ICH compliance. The starting compensation for this job at the Principal Scientist level is a range from $124,520 - $ 150,900, plus ... and e xecute analytical and CMC strategies that ensure safety , quality and efficacy of life - saving medicines...the critically review of regulatory filings including evaluation of data from collaborator labs. + Stay current with industry… more
- Merck (North Wales, PA)
- **Job Description** The Director ( Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving new or ... and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports,… more
- Merck (North Wales, PA)
- … data preprocessing, filtering, and manipulation; programming expertise with clinical endpoint data (efficacy and safety ) and pharmacokinetic data (raw ... programming analyst will gather and interpret user requirements, retrieve the required data , transform the data into modeling-ready analysis datasets, and… more
- Merck (North Wales, PA)
- …data steps, procedures, SAS/MACRO, SAS/GRAPH and programming expertise with clinical endpoint data (efficacy and safety ) and pharmacokinetic data (raw ... with stakeholders (statisticians/modelers) and clinical colleagues, retrieve the required data , transform the data into analysis/modeling datasets, and… more
- Merck (North Wales, PA)
- …the development and execution of statistical analysis and reporting deliverables (eg safety and efficacy analysis datasets, tables, listings, figures), the span of ... multiple stakeholder groups which include clinical development, outcomes research and safety evaluation. The position is a key collaborator with statistics and… more
- Merck (Trenton, NJ)
- …Device Quality & Regulatory Team within Global Regulatory Affairs and Clinical Safety (GRACS). The primary responsibility for this position is to ensure regulatory ... management system, including working with sites to collect, analyze and summarize data for management review meetings and presentations. + Support device related… more
- New York University (New York, NY)
- …Tool (POCOCT), a microfluidics ensemble and single cell image-based data acquisition system employing artificial intelligence with interpretation of >100 ... to join the study team as an Associate Research Scientist / Research Technologist position. The successful candidate will...the obtained findings. Careful documentation of patient cell-based image data will serve as the basis for development of… more
- ThermoFisher Scientific (New Brunswick, NJ)
- …Drug Substance and Drug Products across internal and external manufacturing sites. The principal scientist reports to the Associate Director of GBS and is ... Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required ( safety glasses, gowning, gloves, lab coat, ear plugs etc.) **Job Description**… more
- Bristol Myers Squibb (Princeton, NJ)
- … and oversees safety narratives (if applicable). + Accountable for medical data review of trial data , including eligibility assessment and interpretation of ... with the TA Medical Lead, CT MEG Lead, Clinical Scientist (CS), and Global Trial Manager (GTM) for the...executional delivery of studies (eg, clinical database development, clinical data oversight, site activation, enrollment status, as well as… more
- City of New York (New York, NY)
- …engineering and safety reviews, and drinking water system projects and data surveillance. Guide strategic direction of research on advancements in water ... The Office of Office of Public Health Engineering (PHE) promotes water safety and prevention of waterborne diseases by monitoring NYC drinking water supply… more
- Bristol Myers Squibb (Princeton, NJ)
- …the Clinical Scientist (CS) for medical questions and education (including safety management guidelines) + Holds responsibility for assessment of key safety ... of the Clinical Development Team (CDT) + Conducts medical data review of trial data , including eligibility...-related serious adverse events in partnership with Worldwide Patient Safety and oversees safety narratives + Collaborates… more
- Bristol Myers Squibb (Princeton, NJ)
- …Clinical Trial data to support development, and + Serving as principal functional author for Regulatory submission, study reports, and publications + Provides ... the Clinical Scientist (CS) for medical questions and education (including safety management guidelines) + Assesses key safety -related serious adverse events… more