Novo Nordisk is a global healthcare leader with over 100 years of innovation in diabetes, obesity, and chronic disease treatments. With a presence in 170+ countries, we impact 40+ million patients daily. Our Global Business Services (GBS) in Bangalore supports clinical drug development, ensuring high-quality data for regulatory approvals.
Job Title: Statistical Monitor
Department: Clinical Drug Development (CDD)
Location: Bangalore, Karnataka, India
Employment Type: Full-time
Job Description
As a Statistical Monitor, you will play a key role in Risk-Based Monitoring (RBM) by analyzing clinical trial data to detect unusual patterns, errors, or fraud. You will collaborate with trial teams, data management, and programming experts to ensure data integrity and compliance with GCP guidelines.
Key Responsibilities:
✔ Detect anomalies in clinical trial data using statistical methods (SAS/JMP).
✔ Collaborate with cross-functional teams to resolve data issues.
✔ Develop and enhance statistical monitoring tools and visualizations.
✔ Support training initiatives and knowledge-sharing within the team.
✔ Ensure compliance with GxP and regulatory requirements.
Eligibility & Qualifications
✅ Education: University degree in Life Sciences, Engineering, or related field (B.Sc/M.Sc/MD).
✅ Experience:
- 2+ years in the pharmaceutical industry.
- 1+ year in clinical data analysis/visualization.
- Knowledge of SAS/JMP programming (preferred).
✅ Skills: - Understanding of GCP & clinical research.
- Basic statistical methods and data flow in clinical trials.
- Proficiency in IT systems & data reporting.
Why Join Novo Nordisk?
✨ Global Impact: Contribute to life-changing treatments for chronic diseases.
💼 Career Growth: Opportunities for mentorship & continuous learning.
🌍 Inclusive Culture: Work in a diverse, collaborative environment.
🏆 Top Employer: Recognized as one of the world’s most valuable companies.
