Employer:Bristol-Myers Squibb CompanyPosition:Sr. Clinical Scientist (Ref: 4361)Location:3401 Princeton Pike, Lawrence Township, NJ 08648Duties: Responsible for implementation, planning, and execution of assigned clinical trial activities by drawing on experience with JReview, Spotfire and Clinical Data Workbench; oncology; Medidata Rave Electronic data capture system; trials conducted in Asia/Pacific region; and immune-oncology drug development. Lead, plan, and execute trial level activities for multiple trials with minimal to moderate level of supervision. Collaborate with clinical development lead/clinical trial physician for provision and analysis of data to support future planning. Maintain a thorough understanding of assigned protocols and protocol requirements and educate supporting team members. Plan and lead the implementation all study startup/conduct/close-out activities as applicable. Evaluate innovative trial designs. Protocol and inform consent form development process with minimal guidance, including writing, reviewing, adjudication / resolution of cross functional comments and ensuring high clinical quality. Conduct site-facing activities such as training and serving as primary contact for clinical questions. Conduct activities related to data generation and validation, including case report form design, clinical data review/query resolution; ensure consistent, quality data review by supporting clinical science team. Perform clinical data trend identification and provide trends and escalate questions to Medical Monitor. Develop clinical narrative plan and review clinical narratives. Provide information required by Protocol Manager for development of trial budget, contract research organization scope of work, etc. Review development of site and clinical research associates training materials and presentation at site initiation visit and Investigator meetings and support on Study committee (e.g., data monitoring committee) activities. Drafting/review and validation of clinical study reports and clinical portions of Regulatory Documents. Collaborate and serve as primary liaison between external partners for scientific advice. May work remotely 5 days every 2 weeks within normal commuting distance of Lawrenceville, NJ.Requirements: PhD degree in biomedical sciences or a related field plus 5 years of post-baccalaureate experience reflecting demonstrable ability in the skill set described above. The required skills do not need to be maintained over the full term of required experience.