- Bristol Myers Squibb (Madison, NJ)
- …Team (SDT) and may be a member of the Clinical Development Team (CDT) + Leads medical data review of trial data , including eligibility review + Holds ... work and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Clinical Trial Physician sits within Clinical Development, which is a… more
- JPMorgan Chase (Jersey City, NJ)
- …and the ability to communicate seamlessly across business, product, tech and data scientist teams. **Preferred qualifications, capabilities, and skills** + ... where your expertise will drive the development of cutting-edge Data , Analytics, and AI/ML Platforms. As a Senior...technologies. + Develops secure and high-quality production code, and review and debug code written by others. + Contributes… more
- Bristol Myers Squibb (Madison, NJ)
- …(CDT) * Study-Leader with ability to own/drive study level strategic decisions * Leads medical data review of trial data , including eligibility review * ... of cross-portfolio activities in line with Clinical Excellence, including Protocol Review Committee, support of Business Development activities and Quality and… more
- Coinbase (Trenton, NJ)
- …ensuring long-term maintainability. *What you'll be doing:* Analytics engineer is a hybrid Data Engineer/ Data Scientist /Business Analyst role that has the ... supported. The Analytics Engineering team bridges the gap between data engineering, data science, and business analytics...and engages in dynamic conversation. A human recruiter will review your interview responses, provided in the form of… more
- J&J Family of Companies (Raritan, NJ)
- …and approval of essential documents for regulatory filings. Performs medical safety data review , including evaluation of adverse events and eligibility of ... Team (CFTT). The SRP provide support to a study senior physician, clinical leader (CL) to deliver a trial(s)...for site interactions in partnership with the clinical project scientist (CPS) for medical questions and education (including safety… more
- Taiho Oncology (Princeton, NJ)
- …study sites regarding a patient's eligibility, dose adjustments, and patient's discontinuation. + Perform data review supported by the CRS on an ongoing basis. ... Review of the safety data will be...Scientist (CRS) who will participate in the medical review process and other study related activities in support… more
- Bristol Myers Squibb (Madison, NJ)
- …clinical development strategy + Analyzing, interpreting, and acting on clinical trial data to support development + Serving as principal functional author for ... lifecycle + Manages site interactions in partnership with the Clinical Scientist for medical questions and education (including safety management guidelines) +… more