Bristol Myers Squibb Company

Feasibility Specialist

Princeton, NJ, United States
Oct 07, 2019
Required Education
Masters Degree/MBA
Position Type
Full time
The Feasibility Specialist is an experienced clinical research professional who specializes in clinical trial intelligence and supports enhanced R&D portfolio, program and country planning, clinical trial feasibility, site selection, country target setting and data driven patient recruitment and enrollment forecasting.

The Feasibility Specialist must be able to perform standard deliverable independently, interpret and translate data for Decision Makers and key clinical team members into actionable solutions.
  • Responsible for developing Country, Site, Patient and Clinical Trial Analytic Data strategies
  • Support data-driven solutions for clinical trial planning and deployment
  • Drive Indication, Program and Trial Specific Feasibility Assessments
  • Lead Strategic Country and Site Allocation for Clinical Trials
  • Analyze Data and provide recommendations to optimize trial placement decisions
  • Create Study level trial enrollment forecast
  • Interpret and translate data for key decision makers and stakeholders:
  • Understanding of Regulatory considerations as they relate to trial planning
    Understanding of Disease Epidemiology, Treatment Standards, Patient Treatment Journey, Competitive Trial Intelligence and Industry Trends as if relates to and impact clinical trial planning
  • Advanced understanding or experience with trial operations
  • Ability to use real-world data (RWD) and predictive analytics
  • Translates customer requests into deliverables.
  • Provides ad hoc analysis of trends within and across protocols to identify opportunities for improvement or creating cost effective synergies.
  • Provides support to Clinical teams in preparation of operational review meeting and other oversight committees
  • Supports specific requests for more advanced data insights and decision support.
  • Supports department and organizational initiatives

Customer focus, attention to detail, experience with information systems and clinical trial intelligence and supporting data, extremely proficient with MS Office (Word, ppt), ability to handle multiple projects. Strong analytical competencies. Exposure to, and understanding of, epidemiological, healthcare, commercial, real world and clinical data sets as it relates to clinical trial planning and execution. Forecasting/simulation experience is a plus.