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Responsibilities:
- Lead statistical programming across trials from start-up to submission.
- Validate TLFs, SDTM/ADaM datasets, Define-XML, and SAS programs.
- Provide oversight, mentoring, and ensure quality delivery.
Requirements:
- 8+ years in pharma/biotech/CRO statistical programming.
- Strong SAS, CDISC, SDTM/ADaM, and TFL skills.
- Regulatory submission experience; Oncology/Rare Disease preferred.
About ClinChoice:
- Global CRO with 4,000+ professionals in over 20 countries.
- Culture of continuous training, diversity, and inclusion.
ClinChoice
ClinChoice is a global full-service CRO providing clinical development and functional solutions for pharma, biotech, medical device, and consumer health companies. With over 4,000 professionals across 20+ countries, they value continuous training, diversity, and inclusion.