CLINICAL APPLICATION SPECIALIST III
CLINICAL APPLICATION SPECIALIST III
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Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
Responsibilities:
- 5 yrs of experience in Statistical Programming using SAS preferably in UNIX environment supporting clinical trials data analysis. Enterprise Guide experience is a plus.
- Solid CDISC Standards knowledge and solid Adam programming experience. Oncology TA experience is preferred.
- Experienced in supporting ISS ISE Adam programming and submissions is a plus.
- 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.
- Familiar with CDISC ADAM dataset structure able to produce TLFs.
- strong SAS programming skill SAS MACRO SAS SQL SAS BASE SAS GRAPH.
Requirements:
- At least 10 yr of direct working experiences in pharma clinical trial preferable late phase studies.
- MS in Statistics Computer Science or a related field with 5 years of relevant experience or BS in Statistics Math Computer Science or a STEM related field with 8 years of relevant experience. Have experience on submission package familiar with p21.
- Strong communication work efficiently and deliver task on time.
- SAS certification.
- SAS EG and Unix environment. SAS Studio experience is a plus as well.
- Pharmaceutical or related industry experience with clinical trials.
Additional Information :
All your information will be kept confidential according to EEO guidelines.
Remote Work :
No
Employment Type :
Contract
Employment Type
Contract
