Job Description
- SAS programming experience, preferably in the UNIX environment, supporting clinical trials data analysis. Enterprise Guide experience is a plus.
- Experienced in supporting ISS, ISE ADaM programming and submissions.
- Ability to quickly learn internal macros, processes and interpretresults.
- Team player with excellent communication skills and experience working with stat programmers, statisticians, and data management personnel.
Qualifications
- MS in Statistics, Computer Science, or a related field. or BS in Statistics, Computer Science, or a related field
- Working knowledge of macro programming; Be able to write macros and be able to comprehend existing macros.
- Derived Dataset derivation; knowledgeable about the definition or specification files
- Pharmaceutical or related industry experience with clinical trials
Additional Information
- BA Certifications.
Clinical Research - Entry Level in tn at Unknown Company
This position is listed as full time and onsite.