- 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
- Bristol Myers Squibb (Princeton, NJ)
- …lives. Read more: careers.bms.com/working-with-us . Job Requisition: Senior Principal Scientist , Development DMPK Challenging. Meaningful. Life-changing. ... drug-interaction potential of drug candidates. Working closely with drug safety and clinical pharmacology, Dev DMPK plays a critical...across the globe. PCO is looking for a Senior Principal Scientist to join the Dev DMPK… 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
- 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
- Merck (West Point, PA)
- …process enhancements, and commercial vaccine expansions. We are seeking an experienced Associate Principal Scientist to join the Live Virus Vaccines Lab in West ... facilities and/or production equipment at full scale. Communicating study designs and data driven results to all levels within and across organizations and… 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
- 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