Clinical Data Management Jobs – at Lilly, Apply Now!
Lilly is hiring for the role of Associate/Senior Associate – Clinical Data Management (CDS) in Bangalore, India. This full-time opportunity
is ideal for professionals with 3–5 years of experience in medical coding and clinical data operations. The role focuses on central coding, data validation, database design, regulatory compliance, and collaboration across global clinical trial teams. If you’re from a medical, life sciences, or pharmacy background and have expertise in data flow management and medical coding standards, this is your chance to contribute to innovative clinical research at a global pharmaceutical leader.Job Posting Details
Position: Associate – CDS / Senior Associate – CDS
Location: Bangalore, Karnataka, India
Category: Research & Development
Job Type: Full Time, Regular
Job ID: R-88313
Job location: Bangalore, India
About Company:
Welcome to Lilly, a leading pharmaceutical company dedicated to creating a healthier world. We are currently seeking a talented individual to join our team as an Associate – CDS/Senior Associate – CDS in Bangalore, Karnataka, India. If you are passionate about clinical data management and looking to make a difference, this could be the perfect opportunity for you.
Minimum Qualification Requirements:
- Bachelor’s degree in medical field, Life Sciences, Health Information, Nursing, Pharmacy, or Para-Medics
- 3 to 5 years of experience in medical coding activities
Primary Responsibilities for Clinical Data Management Jobs:
Portfolio Strategy, Planning, and Delivery
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Execute Lilly business requirements for the study/program for vendors to deliver clinical trial data
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Ensure data management deliverables are delivered to scope, cost, and time objectives
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Coordinate end-to-end data management activities – from study setup through trial execution to dataset delivery, including on-time delivery of a quality, locked database
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Ensure flow of data, including across niche vendors and data sources (e.g., PK, immunogenicity, biomarker)
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Contribute to key deliverables: Data Management Plan, Project Plan, databases, observed datasets
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Participate in submission, inspection, and regulatory response activities
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Complete central coding activities
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Archive and decommission study-related data management content
Project Management
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Ensure data acquisition, validation, medical coding, and datasets reflect specific protocol objectives
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Implement and comply with Lilly data standards; provide study/program-specific recommendations
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Track and report study build, execution, and data delivery metrics as Clinical Data Management
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Experienced data managers help create scope scenarios and negotiate outcomes
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Integrate disparate data sources for decision-making
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Apply therapeutic knowledge and technical expertise to ensure database accuracy
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Apply knowledge of regulatory standards (e.g., MHRA, FDA, ICH, GCP, PhRMA, Privacy) to data deliverables
Enterprise Leadership
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Improve processes to reduce cycle time and work effort
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Represent Data and Analytics in cross-functional initiatives as Clinical Data Management
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Participate in shared learning across the Data and Analytics organization
Keywords: Medical coding activities, Clinical Data Management, Lilly, Bangalore, Full Time
