Principal Statistical Programmer

Responsibilities :

• Participate in developing and maintaining clinical trial data and statistical programming standards to ensure the company standards are up to date and in line with pharmaceutical industry standards, conventions, and regulatory requirements.
• Perform hands on primary statistical programming and validation programming on assigned projects including but not limited to phase I – IV clinical trials, integrated clinical summaries, responses to requests from regulatory agencies, publication support, data explorations, data monitoring committee meetings, etc.
• Create SDTM mapping specifications and ADaM data specifications.
• Perform quality control (QC) review of these documents prepared by others.
• Create SDTM and ADaM files.
• Perform QC review of these files prepared by others.
• Perform rd level QC review on programming deliverables before their release to the clients.
• Perform QC review / assessment on regulatory submission programming documents, datasets, tables / listings / graphs (TLGs), and computer programs, etc.
• May lead programming efforts for drug development programs or for assigned client clusters.
• Provide training, mentorship, and technical guidance to less experienced Statistical Programmers or Biostatisticians who perform statistical programming.
• SOPs, guidelines, and good working practices.
• Participate in statistical programming project bidding or bid defense meetings.
• Work with document management specialists / archivists to plan and perform archival of the statistical programming datasets, outputs, documents, and final programs upon the completion of the assigned projects.
• Perform transfer of the archived files to the clinical trial sponsors.

Requirements :