Clinical Application Specialist III

North Chicago, IL - USA

Monthly Salary: Not Disclosed

Posted on: 30+ days ago

Vacancies: 1 Vacancy

Job Summary

Responsibilities:

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.

Requirements:

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.

Responsibilities: 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. Immuno...