Are you an experienced SAS programmer in Clinical Data Management (CDM) looking for a fully remote opportunity? A leading global CRO is hiring a Senior CDM Programmer (SAS) in Bangalore, India. This role offers a chance to lead clinical data programming projects, mentor teams, and deliver high-quality outputs that support clinical trials worldwide.
If you have 5+ years of SAS programming, SQL, and EDC expertise, this could be your ideal next step.
📝 Key Responsibilities
As a Sr. CDM Programmer (SAS), you will:
- Lead data management programming deliverables, ensuring accuracy and compliance.
- Define, import, and validate data within CDM systems.
- Create and test data listings, reconciliation reports, and specialized outputs (e.g., MPRs, SSTs, SAE Reconciliation).
- Develop and maintain DTAs based on standard guidelines.
- Extract and reconcile data from multiple EDC systems.
- Provide mentorship and training to junior programmers.
- Collaborate with cross-functional teams to improve processes.
- Support system troubleshooting and reporting with IT teams.
🎓 Qualifications
- Education: Bachelor’s degree (Pharmacy, Life Sciences, IT, or equivalent).
- Experience: 5+ years in SAS programming for clinical data management.
- Proficiency in SAS, SQL, SpotFire, Crystal Reports, JReview.
- Strong knowledge of relational database systems (RDBMS).
- Understanding of GCP guidelines and SOPs.
- Excellent communication, leadership, and organizational skills.
🌟 Benefits
- Fully Remote work flexibility.
- Work with global teams on cutting-edge clinical trials.
- Opportunities for leadership and mentoring.
- Professional growth in CDM, SAS, and regulatory data programming.
- Competitive salary (₹12,00,000 – ₹20,00,000 per annum).
📌 How to Apply
