Senior Manager, Statistical Programming

Eisai US•Remote, NJ
•$138,800 - $182,200

About The Position

The Senior Manager, Statistical Programming is responsible for SAS programming activities supporting multiple studies for a single compound or multiple compounds within related therapeutic areas. This role owns the programming experience from inception through submission in related areas. The position manages programming projects and works with cross-functional teams and vendors to deliver high-quality outputs on schedule. It also contributes to statistical analysis plan implementation, vendor oversight, process improvement, and team member development.

Requirements

  • Bachelor’s or master’s degree in computer science, public health, biostatistics, statistics, or another related area.
  • At least 8 years of experience with a bachelor’s degree or 5 years with a master’s degree in clinical development statistical programming methods and processes, preferably in pharmaceutical, CRO, academic, or related environments; an equivalent combination of education and experience is also accepted.
  • Experience driving results indirectly by influencing others.
  • Significant vendor management experience.
  • Significant SAS experience.
  • Some experience leading projects involving Phase I and II studies.
  • Significant CDISC (SDTM/ADaM) experience.
  • Proven performance in an earlier or comparable role.
  • Skills in communication and cross-functional influence, critical thinking and business agility, industry and regulatory knowledge, mentoring and people development, project management, statistical programming, and vendor management.

Responsibilities

  • Manage one or more statistical programming projects, working closely with cross-functional teams and vendors to ensure timely delivery of high-quality outputs.
  • Develop and review code, create datasets, and produce summary Tables, Graphs, and Listings (TLGs) according to the Statistical Analysis Plan.
  • Review statistical analysis plans for assigned projects and contribute to their implementation.
  • Collaborate with Biostatistics, Data Management, Clinical Operations, and other teams to ensure dataset and summary accuracy, resolve implementation issues, and represent Statistical Programming in study team meetings.
  • Participate in identifying and selecting external partners and vendors, and monitor the quality of their deliverables.
  • Improve the team’s statistical programming capabilities through process, systems, and tools improvements, as well as training.
  • Mentor less experienced team members.

Benefits

  • Eligible to participate in the Eisai Inc. Annual Incentive Plan.
  • Eligible to participate in company employee benefit programs.
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