Clinical Data Coordinator

Roles & Responsibilities
• Develop and test eCRFs (electronic Case Report Forms)
• Perform data validation and manage clinical data queries
• Prepare and maintain CDM documentation (DMP, DVP, eCCG)
• Conduct data reconciliation and support site/study training activities
• Perform medical coding as per study requirements
• Ensure accurate and timely clinical data management activities
• Coordinate with cross-functional teams for data review and resolution

Qualification
• M.Pharm (Pharmacology / QA)
• BDS / BAMS / BHMS
• Msc (Life Sciences)

Experience
• Site-level experience as Clinical Research Coordinator in late-phase trials
• Experience in EDC systems and related tools (IWRS, ePRO, etc.)
• Hands-on experience in Clinical Data Management activities

Skills
• Strong understanding of clinical trial processes and GCP guidelines
• Knowledge of data validation, query handling, and reconciliation
• Familiarity with medical coding practices
• Good documentation and organizational skills
• Strong communication and teamwork ability
• Attention to detail and data accuracy

About the Organization
Lambda Therapeutic Research is a global full-service CRO headquartered in Ahmedabad, India, providing end-to-end clinical research services to pharmaceutical, biotech, and generic companies worldwide. With operations across India, USA, Canada, UK, Spain, and Poland, Lambda supports innovative clinical development on a global scale.