Senior Statistical Programmer (SDTM)

📋 Description

• Lead SDTM programming on clinical studies, delivering SDTM deliverables.
• Program and deliver complex SDTM datasets per study requirements and standards.
• Develop and review SDTM Trial Design domains and mapping specs.
• Coordinate study start-up activities, defining programming deliverables.
• Review SAPs and protocols, advising on SDTM mapping strategies.
• Perform programming, QC, debugging SAS macros; support analysis and reporting.

🎯 Requirements

• Degree in a relevant discipline or equivalent experience.
• Experience in clinical trials or regulated environments.
• Strong SAS programming skills and SDTM/clinical reporting knowledge.
• SDTM Lead or study/ project lead experience on clinical projects.
• Proven SDTM/ CDISC standards knowledge, mapping, and regulatory submission experience.
• Experience mentoring and collaborating with cross-functional teams.

🎁 Benefits

• Full-time, remote working opportunity in India.
• Exposure to global clinical studies and diverse environments.
• Opportunities to enhance SAS, SDTM, CDISC, and clinical data programming expertise.
• Potential for technical leadership and study coordination roles.
• Mentoring, knowledge sharing, and professional development.
• Collaborative environment with global teams and process improvements.