Clinical Application Specialist III
Clinical Application Specialist III
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Salary Not Disclosed
1 Vacancy
Job Description
- 6 to 8 years of SAS programming experience preferably in UNIX environment supporting clinical trials data analysis.
- Enterprise Guide experience is a plus.
- Solid CDISC Standards knowledge 8 years of ADaM and TLF programming experience supporting safety and efficacy analysis.
- Immunology TA experience is preferable but not required.
- Well experienced in converting information from aCRF SDTM data SAP and SPP into ADaM specifications and review TLF outputs from vendors.
- Experienced in supporting ISS Client ADaM programming and submissions.
- Ability to quickly learn internal macros processes and interpret Pinnacle 21 results.
- Team player with excellent communication skills and experience working with stat programmers statisticians and data management personnel.
- MS in Statistics Computer Science or a related field with 6 years of relevant experience. or BS in Statistics Computer Science or a related field with 8 years of relevant experience.
- SAS certification is nice to have.
- SAS EG and Unix environment.
- Pharmaceutical or related industry experience with clinical trials.
- SAS programming.
- 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.
Employment Type
Full-time
