- Tris Pharma (Monmouth Junction, NJ)
- …has an immediate need for an experienced TEMPORARY Analytical Research and Development Scientist III . This is a temp to possible permanent position.SummaryThe ... Our colleagues understand the criticality of operating a successful business and take pride in the company's success. Equally...Analytical Research and Development (ARD) Scientist III , under guidance, performs laboratory analyses… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for 1 or several complex studies in various settings including Phase I- III , within a delivery model comprising of outsourced studies or outsourced studies ... according to agreed quality standards and timelines and that quality of data is suitable for regulatory submission. The SDL collaborates with cross-functional… more
- Teva Pharmaceuticals (Parsippany, NJ)
- Clinical Scientist , Director Clinical Development Date: Oct 25, 2025 Location: Parsippany, United States, New Jersey, 07055 Company: Teva Pharmaceuticals Job Id: ... new people to make a difference with. **The opportunity** The Clinical Scientist (CS), Director provides scientific expertise necessary to design and deliver… more
- Bristol Myers Squibb (Madison, NJ)
- …+ 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 ... forums as the consulted authority for the disease area, including within Business Development function + Partners with Worldwide Patient Safety physicians in the… more
- Bristol Myers Squibb (Princeton, NJ)
- …Seeking candidates with Biomarker Lead late stage clinical trials for Phases II/ III preferred. Regulatory submissions drug approvals in solid tumor space also highly ... of this role are to act as a lead scientist to implement and deliver on biomarker strategies for...for clinical programs, develop reports and publications on translational data generated to support asset development and contribute to… more
- Bristol Myers Squibb (Madison, NJ)
- …line with Clinical Excellence, including Protocol Review Committee, support of Business Development activities and Quality and compliance leadership. The Clinical ... Clinical Excellence, including eg Protocol Review Committee, support of Business Development activities and Quality and Compliance leadership **Clinical Development… more
- J&J Family of Companies (Raritan, NJ)
- …responsible for site interactions in partnership with the clinical project scientist (CPS) for medical questions and education (including safety management ... approval of essential documents for regulatory filings. Performs medical safety data review, including evaluation of adverse events and eligibility of participants… more
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