

I am a Clinical Research Professional with over 3 years of experience ensuring data integrity, regulatory compliance, and operational excellence in clinical trials. My expertise spans source document verification, electronic data capture (EDC) systems, and quality control processes aligned with ICH-GCP and FDA guidelines.
I am passionate about advancing research and improving patient outcomes through meticulous data management and collaborative team support. My background includes optimizing workflows, supporting timely database locks, and training staff to maintain high standards of compliance and accuracy.
Certified in GCP and CITI, I bring a strong foundation in clinical operations and a results-driven approach to supporting complex psychiatric and surgical trials.
Core Strengths:
✔ Clinical Data Management & Quality Control
✔ Regulatory Compliance (ICH-GCP, FDA)
✔ EDC Systems & CTMS Platforms
✔ Patient Recruitment & Retention Strategies
✔ Staff Training & Process Optimization