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SAS Clinical Trial Programmer Analyst


Reference Number: RKNCSC24

SAS Clinical Trial Programmer Analyst
experience  Not Disclosed
location  Remote, NC (100% Remote)
duration  12.0 Months
salary  Not Disclosed
jobtype  Not Disclosed
Industry  Government - Local
Job Description

Job Description:

Client will provide analytical services in support of customer’s clinical research studies and FDA submission process.

QUALIFICATIONS – ESSENTIAL

• Bachelor’s degree or equivalent, preferably in a scientific discipline such as Statistics, Computer Science, Mathematics, Business Administration, etc. Healthcare or technology related field.
• 4-5+ years of SAS programming experience working with clinical trial data in the Pharmaceutical & Biotech industry.
• SAS certifications (Base, Advanced, etc.) are highly desired.
• Strong SAS Macro Language experience and knowledge.

MAJOR RESPONSIBILTIES/ACTIVITIES:

• Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming.
• Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs).
• Production and QC / validation programming.
• Generating complex ad-hoc reports utilizing raw data.
• Applying strong understanding/experience with Efficacy analysis.
• Performing lead duties when called upon.
• Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc..
• Excellent written and spoken communication skills


Working Arrangement: 100% remote
VIVA is an equal opportunity employer. All qualified applicants have an equal opportunity for placement, and all employees have an equal opportunity to develop on the job. This means that VIVA will not discriminate against any employee or qualified applicant on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status

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