What are the responsibilities and job description for the Clinical Application Specialist III position at Katalyst CRO?
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.
- 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.
