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.