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.

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