Supriya Tadepalli

Life Sciences postgraduate with hands-on exposure to clinical research and clinical trial support, including protocol-driven study activities, CRF design and review, EDC systems (Medidata Rave, Oracle Clinical, Castor EDC), and study documentation in compliance with ICH-GCP and SOPs. Brings 6 months of experience in regulated healthcare data operations and medical coding, strengthening clinical terminology, data accuracy, and quality standards. Demonstrated ability to support clinical trial setup, data validation, query management, audit readiness, and cross-functional collaboration.

Highly motivated to begin a long-term career as a Research Consultant (Clinical Research Associate) through structured training and on-site project execution.

Junior Executive Medical Coder at CorroHealth (2025-07 – 2026-01)

Medical coding and healthcare data validation in regulated environment

• Validated 1000+ clinical records ensuring 98% accuracy and 100% HIPAA compliance across submissions
• Maintained structured healthcare data records and supported internal QA reviews and audits, contributing to improved data quality and reduced rework
• Applied ICD-10-CM coding standards across 1,200+ patient records, meeting required quality and productivity benchmarks
• Consistently met data privacy, documentation, and submission timelines throughout a 6-month tenure in a regulated environment
• Tracked 50+ performance metrics weekly, documented procedures improving data retrieval speed by 20%

Clinical Data Management Trainee at Biotecnika (2025-03 – 2025-07)

Clinical data management and EDC platform support for clinical trials

• Supported protocol-aligned clinical trial database setup and configuration using EDC platforms (Medidata Rave, Oracle Clinical, Castor EDC) in alignment with study protocols and SOPs
• Performed clinical data entry, data validation, and data review across 25+ CRF pages/forms, maintaining high data accuracy and consistency
• Assisted in the design, review, and validation of 20+ Case Report Forms (CRFs) to ensure protocol-compliant and efficient data capture
• Created and maintained study tracking logs, system documentation, and study records, supporting ongoing study monitoring and audit readiness
• Conducted data cleaning, discrepancy management, query generation, and query resolution, resolving 150+ data queries and supporting improved data quality outcomes
• Reviewed audit trails and system reports to ensure compliance with ICH-GCP guidelines, regulatory requirements, and data integrity standards throughout the study lifecycle
• Gained hands-on exposure to CTMS and EDC workflows for study tracking and project coordination

Master of Science (M.Sc) in Microbial Technology – Reva University, Bengaluru (2023 – 2025)

Bachelor of Science (B.Sc) in Life Sciences – Jyoti Nivas College Autonomous, Bengaluru (2020 – 2023)