Job Title

Key Responsibilities - Develop and validate complex analysis datasets (ADaM) and TFLs using SAS. - Write and review programming specifications and supporting documentation. - Create standard macros and tools to improve efficiency. - Serve as a project lead programmer, assigning tasks, managing timelines, and providing technical guidance to junior team members. - Communicate with clients as the key programming contact, including delivering outputs and managing feedback. - Conduct SAS code review, track issues, and ensure quality standards are met. - Archive all programming deliverables and documentation per SOPs. - Mentor team members and support their technical and professional development. - Ensure compliance with ICH-GCP, CDISC standards, and company SOPs. Requirements - Bachelors degree or above in Statistics, Mathematics, Computer Science, or related field. - 5+ years of SAS programming experience in pharmaceutical or CRO environments. - Strong knowledge of clinical trials, statistical methods, and regulatory requirements. - Proven experience leading programming projects and mentoring team members. - Excellent communication skills and experience working with global teams and clients. - Proficient in SAS software.