Job Description:

• Oversee all phases of data management, quality control, and reporting for research projects including clinical trials.
• Define analytical variables collaboratively with research scientists and biostatisticians.
• Consult with project staff on project needs.
• Maintain a professional relationship with project personnel.
• Perform analytical tasks using SAS or other analytical tools.
• Design comprehensive quality checking and validation process.
• Design troubleshooting software and programs.
• Design and generate tracking and data entry tools as needed.
• Design automated reporting and data loading schemes.
• Convert and merge data with complicated structure from a wide variety of sources across platforms.
• Create and maintain documentation to document process and data quality issues.
• May supervise the work of lower level SAS Analyst/Programmers serving on the same projects.
• Perform other related duties incidental to work described herein.

Qualifications:

• Minimum three (3) years of related experience with programming and data management using SAS or other computer language.
• Bachelor\\\'s degree in computer science, biostatistics, statistics, mathematics, information systems, epidemiology or related field of study.License, Certification, Registration
• N/A

Key Skills: