Description
<p><b>Key Responsibilities</b></p><ul><li>Develop and validate complex <b>analysis datasets (ADaM)</b> and <b>TFLs</b> using SAS.</li><li>Write and review <b>programming specifications</b> and supporting documentation.</li><li>Create <b>standard macros</b> and tools to improve efficiency.</li><li>Serve as a <b>project lead programmer</b>, assigning tasks, managing timelines, and providing technical guidance to junior team members.</li><li>Communicate with clients as the <b>key programming contact</b>, including delivering outputs and managing feedback.</li><li>Conduct <b>SAS code review</b>, track issues, and ensure quality standards are met.</li><li>Archive all programming deliverables and documentation per SOPs.</li><li>Mentor team members and support their technical and professional development.</li><li>Ensure compliance with <b>ICH-GCP</b>, CDISC standards, and company SOPs.</li></ul><p><b>Requirements</b></p><ul><li><b>Bachelor’s degree or above</b> in Statistics, Mathematics, Computer Science, or related field.</li><li><b>3+ years of SAS programming experience</b> in pharmaceutical or CRO environments.</li><li>Strong knowledge of <b>clinical trials</b>, <b>statistical methods</b>, and <b>regulatory requirements</b>.</li><li>Proven experience <b>leading programming projects</b> and mentoring team members.</li><li>Excellent <b>communication skills</b> and experience working with global teams and clients.</li><li>Proficient in <b>Microsoft Office</b> and <b>SAS software</b>.</li></ul><p></p>
