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Job Description
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
- Bachelor’s 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.