- Mondelez International (East Hanover, NJ)
- …**Join our Mission to Lead the Future of Snacking. Make It With Pride.** The Sr . Scientist II will execute the Scientific Affairs Strategy for your ... respective categories and geographical area using your Scientific and Regulatory expertise. You advocate for our regulatory ...and Regulatory expertise. You advocate for our regulatory and scientific positions to promote the removal of… more
- Astrix Technology (Essex County, NJ)
- ** Sr Staff Scientist - Medical Device** Science & Research Essex County, NJ, US Pay Rate Low: 128000 | Pay Rate High: 184000 + Added - 27/05/2025 Apply for Job ... $128K- $184K DOE **Travel Requirement:** ~10% **Position Overview:** We are seeking a Sr . Staff Scientist to lead the technical strategy and execution of… more
- Bristol Myers Squibb (Madison, NJ)
- …Ensures studies are aligned with target label indications and are designed to meet regulatory , quality, medical, and access goals * Serves as a matrix leader to ... + May serve as CTP as necessary + Accountable in partnership with the Clinical Scientist for the design, execution, and analyses of each study led by the CTPs and… more
- Bristol Myers Squibb (Madison, NJ)
- …and will supervise and have accountability for the clinical components of regulatory filings. * Will contribute to overall Therapeutic Area disease strategy while ... asset/drug, disease area (rheumatology) and relevant science in order to meet regulatory and disease strategy targets. * Done in conjunction with Clinical… more
- J&J Family of Companies (Raritan, NJ)
- …credible relationships with opinion leaders, medical directors, and key regulatory officials. **Supervision:** Senior study physician/Trial Clinical Leader ... 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
- Bristol Myers Squibb (Madison, NJ)
- …medical accountability and oversight for multiple clinical trials + Manages Phase I/ II studies, with demonstrated decision making capabilities + Provides medical and ... to support development, and + Serving as principal functional author for Regulatory submission, study reports, and publications + Provides oversight and medical… more