Deepak T

About Deepak T

With over 10 years of experience in Clinical Data Management, I currently serve as a Data Team Lead at IQVIA, driving excellence across global clinical trials. My career has been built on a strong foundation of ICH-GCP principles, regulatory compliance, and the drug development process, ensuring data integrity and operational efficiency throughout the study lifecycle.I bring hands-on expertise in- Clinical Documentation & Compliance: Drafting eCRFs, developing Data Management Plans (DMPs), Data Validation Plans, and ensuring accurate archiving in eTMF- System Validation & Quality Assurance: Conducting edit check testing, UAT, and system validation to uphold the highest data standards- Trial Lifecycle Management: Successfully managing Database Locks, Interim Locks, and Analysis across all phases of clinical trials- Oncology Studies: Specialized in handling oncology trials using RECIST and WHO criteria, with experience in centralized and risk-based monitoring approaches.Throughout my career, I have collaborated on global projects across multiple phases of clinical trials, consistently delivering results while fostering compliance, efficiency, and stakeholder trust. My passion lies in leveraging data to accelerate drug development and improve patient outcomes.

Experience

1. Data Team Lead

   IQVIA

   Jan 2026 — Present · Thane, IN

Education

• VIT university

  Master of Science (M.Sc.), Biotechnology

  2010 — 2015

• Vellore Institute of Technology

  Master's degree, Biotechnology

  2010 — 2015

Skills

• Pcr
• Management
• Sas
• Proofreading
• Clinical Trial Analysis
• Microsoft Excel
• Hplc-Ms
• Microsoft Office
• Microsoft Word
• Data Analysis
• Medidata
• Clinical Research
• Data Validation
• Biotechnology
• Dna Electrophoresis
• Molecular Biology
• Oncology Clinical Research
• Project Management
• Centrifugation
• Clinical Trials
• Research
• Standard Operating Procedure (Sop)
• Rt-Pcr