At Clario, a part of Thermo Fisher Scientific, our Cardiac Solutions team supports clinical trials worldwide through the delivery of high-quality statistical programming, analysis datasets, and regulatory submission packages. As a Statistical Programmer, you will play a key role in developing and validating CDISC-compliant datasets, supporting cardiac safety analyses, and ensuring regulatory-ready deliverables are produced with accuracy and efficiency. This role is ideal for a cooperative programming professional who enjoys working with clinical trial data and contributing to the development of life-changing therapies.
What We Offer
Competitive pay and incentives
Provident fund and medical insurance
Engaging employee programs and local events
Contemporary office spaces and work from home flexibility
What You'll Be Doing
Produce, validate, and maintain submission-ready datasets to support cardiac safety clinical trials, including SDTM ECG (EG) and ADaM ADEG datasets.
Create, test, and maintain SAS programs used to generate and validate CDISC-compliant datasets.
Develop, test, and implement data standards that support cardiac research and regulatory submissions.
Perform double programming and validation activities to ensure the accuracy of statistical analysis datasets.
Generate and interpret compliance checks for CDISC-formatted datasets, including SDTM and ADaM standards.
Support research initiatives by providing programming expertise and analysis results to senior team members and department leadership.
Create electronic submission packages, including Define.xml, reviewer guides, and supporting regulatory documentation in accordance with FDA submission requirements.
Train team members on standard operating procedures, programming standards, and best practices.
Identify and implement process improvements to enhance operational efficiency and data quality.
Manage project timelines and client commitments to ensure on-time delivery of assigned de