Bristol-Myers Squibb Company

Associate Director of Clinical Trial Analytics

Location
Princeton, NJ, US
Posted
Jan 19, 2019
Ref
R1512182
Required Education
Masters Degree/MBA
Position Type
Full time
  • 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