Senior Clinical Analyst and Programmer

📋 Description Lead programming for clinical data review, safety monitoring, and centralized monitoring. Develop and maintain clinical data listings, reports, and programming solutions. Analyze Data Management and RBM requirements to deliver timely programming solutions. Create listing specifications from user requirements, protocols, EDC databases, and data validation. Develop SAS-based data review and safety listings for clinical studies. Document programming changes and processes to quality standards. 🎯 Requirements Bachelor’s degree in Science or related discipline required. Minimum 10 years of clinical research experience in biotech/pharma/CRO. At least 5 years hands-on SAS programming experience. Strong understanding of clinical trial data, SAS datasets, database specs, and development processes. SAS certification or Advanced Programmer certification is preferred. Excellent English communication and ability to work with global teams. 🎁 Benefits Fully remote home-based position in India. Permanent full-time employment opportunity. Flexible work schedule supporting work-life balance. Contribute to global clinical research programs. Exposure to advanced clinical data management and programming practices. Continuous learning and professional development opportunities.