Bristol Myers Squibb Associate Director of Clinical Trial Analytics in Princeton, New Jersey

  • Leads a team of specialists who are in charge of clinical trial enrollment/randomization, performance forecasting and tracking for Phase I to IV clinical trials across all therapeutic areas

  • Provides strategic leadership and oversight for the analytic aspects of the clinical trial performance at all stages of drug development at a variety of internal forums, increase understanding of metrics and forecasts, particularly with respect to timeline analytics

  • Responsible for resource utilization and demand management in the Metrics and Reporting group

  • Represents the Clinical Trial Analytics perspective across GCO and beyond

  • Interacts with Operations Leads, Protocol Managers, Site Managers and other stakeholders as appropriate

  • Provides strategic direction and oversees the creation of recruitment dashboards, enrollment projections, Eclipse reports, and ad hoc custom outputs

  • Manages vendor relationships, creates strategy for long term engagement and identifies solutions for short term deliverables

  • Dynamically leverages the existing contractor pool to maximize performance and manage workload peaks.

  • Fully responsible for the assigned team’s development, coaches and mentors them according to their needs

  • Accountable for driving continuous improvement and innovation in the Metrics and Reporting team and at the CT Analytics level. Identifies areas for improvement and acts as a sponsor or contributor to work streams and other CI initiatives.

  • Strategic planning and coordinated implementation of Digital Health partnership projects, and building a comprehensive analytic ecosystem for better trial planning and execution support

Qualifications

Requirements:

  • Masters degree in public health, epidemiology, health care or other life-sciences.

  • 5+ years experience in clinical trial management or clinical trial information support.

  • Strong understanding of clinical trial processes.

  • Experience with country and site selection, trial feasibility, performance tracking and vendor management.

  • Experience with Digital Health activities including RWD/EMR, patient matching, precision Site and Country selection

  • Experience with strategic solution planning, vendor selection and integrated implementation

Skills:

  • Strong people management and inter-personal skills.

  • Excellent presentation of insights

  • Customer focus

  • Attention to detail

  • Experienced with information systems and clinical trial intelligence and supporting data

  • Extremely proficient with MS Office (Word, Excel, ppt). VBA, ORACLE, SAS or R is a plus

  • Ability to handle multiple projects

  • Strong analytical competencies

  • Exposure to, and understanding of epidemiological, healthcare, commercial and clinical data sets as it relates to clinical trial planning and execution

Bristol-Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.