Sravanth V

About Sravanth V

A meticulous and well-organized clinical research coordinator with over 2+ years of experience managing clinical trials from Phase I to Phase IV across various therapeutic areas, including cardiology, oncology, and neurology, in compliance with ICH/FDA regulations. Skilled in collaborating with investigator sites, managing regulatory documentation, and ensuring adherence to research protocols. Proven ability to build strong working relationships with research teams, investigators, and study participants. Committed to advancing medical knowledge and improving patient care through ethical and innovative research practices.

Experience

1. Clinical Research Coordinator

   Research Center For Clinical Studies, Inc

   Sep 2023 — Present · US

   Coordinated multiple Phase II and clinical trials using REDCap and Medidata Rave for real-time data entry and query resolution, achieving 100% accuracy in EDC data verification during monitoring visits.o Managed subject recruitment and retention for trials across therapeutic areas, utilizing Epic EHR to pre-screen candidates, increasing enrollment efficiency by 25% within the first quarter.o Oversaw regulatory compliance by preparing IRB submissions and ensuring adherence to FDA, GCP, and HIPAA standards, resulting in zero protocol deviations or audit findings.o Collaborated cross-functionally with investigators, sponsors, and monitors through Veeva CTMS and Florence eBinders, streamlining document management and reducing startup timelines by 15 days.o Conducted source data verification (SDV), AE/SAE documentation, and investigational product (IP) accountability with strict adherence to ICH-GCP and Informed Consent requirements.o Utilized Microsoft Excel and PowerPoint for patient tracking, trend analysis, and weekly study progress presentations to PI and sponsor teams.

Education

• Sacred Heart University

  Master, Health Care Informatics

• KNR university

  Bachelor, Dental Surgery