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Accountabilities:
- Lead statistical programming activities for Phase I–IV clinical studies.
- Develop and maintain CDISC-compliant SDTM and ADaM specifications.
- Mentor junior programmers and support regulatory submissions.
Requirements:
- Bachelor's degree in Statistics, Computer Science, or related field.
- 4+ years of clinical data programming experience.
- Strong SAS programming skills and knowledge of CDISC standards.
Benefits:
- Remote or hybrid work flexibility within India.
- Opportunity to contribute to global clinical development programs.
- Professional growth opportunities through technical leadership.
Unknown
The partner company is a clinical research organization focused on driving healthcare innovation through clinical trials. The company's size and culture are not specified in the posting.