We are actively seeking highly experienced Statistical Programmers to join our growing team. This role is ideal for professionals with deep domain expertise in clinical trial programming and hands on experience on efficacy datasets and output
? Key Responsibilities:
Develop and validate ADaM datasets and TFLs (Tables, Figures, Listings) in compliance with CDISC standards
Collaborate with statisticians, data managers, and cross-functional teams to ensure timely delivery
✅ Required Qualifications:
✅ 10+ years of experience in Statistical Programming within clinical trials
✅ Strong expertise in ADaM and TFL programming
✅ Minimum 2 years of lead/mentorship experience
✅ At least 1 year of hands-on R programming experience
✅ Solid knowledge of CDISC standards and regulatory requirements
⭐ Preferred:
Experience supporting Phase II and Phase III clinical trials
Excellent problem-solving, communication, and stakeholder management skills
Candidates who are interested, kindly forward your updated resume to
- Be part of something bigger. Be part of IQVIA. ?