- Kuala Lumpur Federal Territory Malaysia

Working Location
Job Description
Responsibilities
Every clinical trial generates vast amounts of data, but raw data alone has little value unless it can be transformed into meaningful, accurate, and compliant information. Behind every successful clinical study are professionals who ensure data is properly structured, validated, and prepared for analysis.
We are looking for an Associate SAS Programmer to join a growing clinical research team. This is an excellent opportunity for individuals who enjoy working with data, programming, and problem solving while building a long term career within the pharmaceutical, healthcare, and clinical research industry.
In this role, you'll be involved in transforming clinical trial data into industry standard formats, supporting statistical programming activities, and ensuring datasets meet regulatory and quality requirements. You'll work closely with statisticians, programmers, data managers, and cross functional teams to support the successful delivery of clinical research projects.
This position offers structured training, hands on exposure to industry standard programming practices, and the opportunity to develop expertise in SAS programming, SDTM conversion, CDISC standards, data validation, and clinical trial data processing. Successful candidates will also undergo six months of on the job training in Guangzhou, China, providing valuable international exposure and professional development opportunities.
Whether you're an early career programmer, a fresh graduate with strong technical foundations, or someone looking to build a specialized career within clinical research, this role provides an excellent platform for growth and development.
Requirements
If you're passionate about data, programming, and working in a highly specialized industry that contributes to healthcare innovation, we'd love to hear from you.
Pay: RM4,500.00 - RM6,000.00 per month
Benefits:
Work Location: In person
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