- Merck (Rahway, NJ)
- …understanding of worldwide regulatory requirements and clinical trial expertise from phase II to V. + Excellent oral and written communication skills and strong ... leadership in a team environment. + Demonstrated ability in statistical research activities and in application of novel methods to clinical trial development. + Publications in peer reviewed statistical/medical journals. + Must also demonstrate the ability to… 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 ... Holds responsibility for site interactions in partnership with the Clinical Scientist (CS) for medical questions and education (including safety management… more
- Bristol Myers Squibb (Princeton, NJ)
- …medical accountability and oversight for multiple clinical trials + Manages Phase I/ II studies, with demonstrated decision making capabilities + Provides medical and ... on Clinical Trial data to support development, and + Serving as principal functional author for Regulatory submission, study reports, and publications + Provides… more