Clinical SAS Programmer - Katalyst Healthcares & Life Sciences
South Plainfield, NJ 07080
About the Job
Responsibilities and Requirements:
- 8 years of experience in clinical trial data analysis using SAS. Preferably in UNIX environment Familiar with Unix command and environment.
- Deep knowledge of CDISC Standards and solid ADaM programming experience. Oncology TA experience is preferred.
- Ability to quickly learn internal macros, processes and interpret Pinnacle 21 results.
- Experienced in supporting ISS, Client ADaM programming and submissions is a plus.
- Team player with excellent communication skills and experience working with stat programmers, statisticians and data management personnel.
- SAS programming, familiar with SAS language modules e.g. SAS MACRO, BASE, SGPLOT, SQL.
- Working knowledge of macro programming; Be able to write macros and able to comprehend existing macros.
- Derived Dataset derivation; knowledgeable about the definition or specification files.
- High degree of technical competence and communication ability, both oral and written.
- Pharmaceutical or related industry experience with clinical trials.
Source : Katalyst Healthcares & Life Sciences