- Merck (Rahway, NJ)
- …in accordance with regulatory, company, and customer requirements. ** Principal Responsibilities** + Lead/Support continuous improvement initiatives for design ... Regulatory teams to ensure compliance with applicable global regulations. + Leverage data analytics and key performance indicators to monitor process performance. +… more
- Merck (Rahway, NJ)
- …Statistics. + Lead the interaction with Clinical, Regulatory, Statistical Programming, Data Management, and other Scientists from our Research & Development Division ... solutions and carries them out. + Develops individual protocols and data analysis plans and independently determines appropriate statistical methodology for… more
- Merck (Rahway, NJ)
- …span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. The incumbent is responsible for the ... experience in developing analysis and reporting deliverables for R&D projects ( data , analyses, tables, graphics, listings) + Strong project management skills;… more
- Pacific Northwest National Laboratory (Trenton, NJ)
- …a strong technical foundation in power and energy systems and advanced data analytics to drive innovation, transform markets, and shape energy policy. ... **Responsibilities** We are seeking a forward-thinking Senior Research Scientist with experience applying Artificial Intelligence (AI), including Large Language… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …working closely with Disease Area Head, Clinical Development Lead, Clinical Scientist . and other functional areas such as GCO, biostats, regulatory, ... final protocol and protocol amendments. + Ensure continuous medical review of aggregated data during clinical trial conduct to identify trends and ensure quality … more
- Merck (Rahway, NJ)
- **Job Description** ** Principal Scientist (Director) - Outcomes Research - Head & Neck cancers** + This position resides within our company's Value and ... with internal teams and external partners, design non-interventional and data synthesis studies, author study protocols, develop measurement questionnaires, case… more
- Bristol Myers Squibb (Madison, NJ)
- …significant, non-significant deviations etc.) * Existing strong relationships with principal investigators. Identifies and cultivates thought leaders in order to ... landscape * The CTP should be able to anticipate impact of external data which may shift internal clinical strategy and proactively assess needs for internal… more
- Noblis (Atlantic City, NJ)
- …Scientific Expertise:** Model Based Systems Engineers (MBSE), Implementation and Test Engineers, Principal Engineer / Scientist / Aviation Specialist, Spectrum / ... Manager, Deputy Program Manager, Project Manager, Task Order Manager, Principal Program Management Specialist, Strategic Planner, Scheduler, Program Analyst, Program… more
- Bristol Myers Squibb (Madison, NJ)
- …Clinical Trial data to support development, and + Serving as principal functional author for Regulatory submission, study reports, and publications + Provides ... and more effective drug development informed by core scientific principles and data . **Functional Area Description** The Early Clinical Development - HOCT function… more
- Bristol Myers Squibb (Madison, NJ)
- …and may be a member of the Clinical Development Team (CDT) + Leads medical data review of trial data , including eligibility review + Holds responsibility for ... site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including safety management guidelines) + Holds responsibility… more