Prashanth Rathnagari
Clinical Research - Life Sciences @Tata Consultancy Services
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WORK HISTORY
Clinical Research - Life Sciences @Tata Consultancy Services
IN
Supporting Phase immuno-oncology and hematology clinical trials, including CAR-T cell therapy programs.Performing Interim Monitoring Visits (IMVs) with focus on patient safety and data quality.Conducting SDV/SDR for eligibility, dosing, safety labs, and follow-up visits using Medidata Rave.Reviewing Informed Consent Forms (ICF) for version control and re-consent compliance.Reviewing and verifying AE/SAE documentation and ensuring timely reporting and follow-up.Performing investigational product (IP) accountability and temperature log review.Maintaining Investigator Site File (ISF) for audit readiness.Worked within centralized oversight while retaining on-site verification and compliance ownership.
EDUCATION
Kakatiya University, Warangal
Integrated Msc Biotechnology , Biotechnology
ABOUT PRASHANTH RATHNAGARI
Clinical Research Associate with 1.5+ years of experience supporting immuno-oncology and hematological malignancy (blood cancer) clinical trials.Currently involved in Phase II and Phase studies, including CAR-T cell therapy programs, with hands-on experience in interim monitoring visits (IMVs), source data verification (SDV), protocol compliance, AE/SAE review, investigational product accountability, and regulatory documentation.Proficient in Medidata Rave EDC and certified in ICH-GCP E6(R3). Experienced in working with investigator sites to ensure patient safety, data quality, and audit readiness across oncology trials.Open to site travel as per study requirements.
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