Eli Lilly and Company is a global healthcare leader committed to discovering life-changing medicines. Headquartered in Indianapolis, USA, Lilly focuses on innovative treatments for diabetes, oncology, immunology, and neurodegenerative diseases. With a strong emphasis on research & development, the company fosters a culture of collaboration, integrity, and patient-centric innovation.
📍 Location: Bangalore, Karnataka, India
📌 Job Type: Full-Time, Regular
🔍 Job ID: R-88313
Job Description: Associate/Senior Associate – CDS (Medical Coding)
Purpose of the Role:
The Clinical Data Management Associate will oversee medical coding activities for clinical trials, ensuring compliance with MedDRA/WHO-DD standards, data quality, and regulatory requirements. The role involves collaboration with data analysts, study teams, and vendors to deliver accurate and timely clinical trial data.
Key Responsibilities:
✔ Medical Coding & Data Management:
- Perform trial-level medical coding (adverse events, medications, medical history)
- Ensure data validation, review, and quality checks
- Support dataset delivery, database lock, and regulatory submissions
✔ Study Execution & Compliance:
- Implement Lilly data standards and ensure ICH-GCP compliance
- Contribute to Data Management Plans (DMP), CRF design, and validation checks
- Manage data flow from niche sources (PK, biomarkers, immunogenicity)
✔ Stakeholder Collaboration:
- Work with clinical data associates, programmers, and analytics teams
- Facilitate data integration for decision-making
- Support inspection readiness & regulatory responses
✔ Process Improvement:
- Optimize data workflows to reduce cycle time
- Engage in cross-functional initiatives & shared learning
Eligibility Criteria
✅ Education:
- Bachelor’s degree in Medicine, Life Sciences, Pharmacy, Nursing, or Health Information
✅ Experience:
- 3-5 years in medical coding (MedDRA/WHO-DD)
- Experience in clinical data management (CDM) & EDC systems (e.g., Rave, Veeva)
- Knowledge of regulatory standards (FDA, ICH-GCP, MHRA)
✅ Skills:
- Strong attention to detail
- Proficiency in medical terminology & coding dictionaries
- Ability to manage multiple trials & deadlines
Why Join Eli Lilly?
✨ Global Impact: Work on cutting-edge clinical trials improving patient lives
💼 Career Growth: Opportunities in pharma R&D, data science, and leadership
🌍 Inclusive Culture: Equal opportunity employer with diversity & inclusion initiatives
🏆 Employee Benefits:
- Competitive salary & bonuses
- Health & wellness programs
- Learning & development opportunities
