Posted: 2 hours ago
Job Description
<p><b>Key Responsibilities</b></p><ul><li>Develop and maintain <b>SAS programs</b> for generating ADaM datasets and TFLs.</li><li>Perform <b>quality control and validation</b> on programs developed by others.</li><li>Collaborate with statisticians and data managers to ensure data accuracy and consistency.</li><li>Create and maintain <b>programming specifications</b> and supporting documents.</li><li>Participate in <b>SOP/WPD compliance</b> and continuous process improvement initiatives.</li><li>Support ad-hoc data requests, clinical data reviews, and data validation activities.</li><li>Continuously improve programming and clinical trial knowledge through training and mentoring.</li></ul><p><br></p><p><b>Qualifications</b></p><ul><li><b>Bachelor’s or above</b> in Statistics, Biostatistics, Mathematics, Computer Science, or related field.</li><li><b>1–2 years</b> of SAS programming experience in clinical trials (pharma or CRO preferred).</li><li>Strong understanding of <b>clinical trial statistics</b> and <b>regulatory guidelines</b>.</li><li>Ability to work <b>independently</b> on assigned projects.</li><li>Proficiency in <b>Microsoft Office</b> and statistical software.</li><li>Good communication skills in <b>English</b> (written and spoken).</li><li>Strong teamwork and documentation skills.</li></ul><p></p>
