Clinical SAS Programmer

Company Description

Katalyst Healthcares & Life Sciences is hiring candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.

Writing SAS programs to create data sets, tables, figures, and listings reporting
Utilizing SAS language, procedures, and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and SAS/GRAPH.
Programming all aspects of a clinical trial, from files to tables and figures
Using SAS in a quality control/ production capacity
Write and edit programs to clean, manage, merge, and analyze data.
Base SAS Certification and SAS advance certification is a plus.
SAS clinical programmer with a minimum of 0-1 years of SAS clinical experience.
CDISC, SDTM and ADaM.
Configure and maintain secure servers in accordance with HIPAA regulations.
FDA Industry Guidelines, ICH Guidelines, and Regulatory Approval Process·
Technical expertise and an excellent working knowledge of Microsoft Office: PowerPoint, Word, Excel, share sites.
Good written and oral communication skills
Ability to work collaboratively as part of a team.
Self-motivation and the ability to drive results independently
Excellent organizational and problem solving skills.

Education: BS/MS degree in Statistics, Biostatistics, Epidemiology or related healthcare and life science fields like Pharmaceutical Science, Regulatory Science, Biology, Chemistry, microbiology, biochemistry with strong analytic skills.

All your information will be kept confidential according to EEO guidelines.