SAS/A Programmer,Loc:San Diego, California,Dur:6M+,Rate:Open

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