Sai Chandini Ravi

About Sai Chandini Ravi

Clinical Research Coordinator (CRC) with a Pharm.D background and hands-on experience in hospital-based clinical trials. Skilled in patient screening, informed consent, protocol adherence, ICH-GCP compliance, and clinical research documentation to support ethical and efficient study conduct.I coordinate with principal investigators, sub-investigators, clinical teams, and sponsors to ensure smooth trial execution, maintain source documents, CRFs/eCRFs, patient logs, and study files, while prioritizing patient safety and data accuracy.With certifications in ICH-GCP and Clinical Trial Design, I contribute to evidence-based research through meticulous attention to detail, effective communication, and proactive problem-solving, committed to upholding ethical standards and patient-centric practices across all studies.

Experience

1. Clinical Research Coordinator

   AIG Hospitals

   Sep 2025 — Present · Hyderabad, IN

   Coordinating clinical trial activities according to study protocols• Conducting patient screening and eligibility assessment• Obtaining and documenting informed consent from participants• Preparing and maintaining source documentation and Case Report Forms (CRFs)• Maintaining the Trial Master File (TMF) and essential study documents• Ensuring compliance with ICH-GCP guidelines and regulatory requirements• Coordinating with investigators, sponsors, and monitors for smooth trial execution• Supporting site monitoring visits, audits, and inspections• Participating in data verification and query resolution to ensure accuracy• Assisting in patient follow-up and documentation of adverse events

Education

• Osmania University

  Doctor of Pharmacy, Pharm D

  2018 — 2024

• Narayana Junior College

  Intermediate , Bipc