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.
SAS certification.
Group setting
SAS EG and Unix environment.
SAS Studio experience is a plus as well.
Pharmaceutical or related industry experience with clinical trials.
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 Client 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.
Top Skills:
Dataset and TLF generation and validation for clinical trials using SAS.
CDISC knowledge familiarity with ADaMIG ADaM specification experience.
Understand study documents and common safety and efficacy analyses.
Teamwork effective communication.
Oncology Therapeutic Area experience or knowledge.
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.