Vedika Rawat profile photo 1 on Tal

Vedika Rawat

Clinical Research Coordinator

Delhi

1+ year of work experience

University College of Medical Sciences and GTB Hospital
Nov 20257 mosPresent

On-site

Clinical Research Network India
Mar 20254 mosJun 2025

Noida, Uttar Pradesh, India

- Conducted participant screening using protocol-defined clinical criteria - Obtained informed consent and maintain enrollment records - Prepared and organized study-specific source documents - Accurately entered source data into the Electronic Data Capture (EDC) system - Coordinated and supported monitoring visits and resolved data queries - Scheduled participant visits and managed study follow-ups - Track, assess, and report adverse events (AEs/SAEs) promptly

Education

Swami Rama Himalayan University

Master of Science - MS, Clinical Research

Swami Rama Himalayan University

20232 yrs2025

Join Vedika and 10k+ other professionals on

Tal Boss

Tal is the app where bosses meet engineers & builders directly, without middlemen

Download Tal Boss

Vedika Rawat on Tal

Headline

Clinical Research Coordinator

About

I am a clinical research fresher with a keen interest in conducting safe, ethical, and impactful studies. I have experience working on clinical trials, managing study documents, coordinating with sites and teams, and ensuring that research runs smoothly and follows all guidelines. I enjoy learning new things in the field of research and always aim to grow my skills and contribute to better treatments for patients. I am open to connecting with professionals in clinical research to share ideas, learn, and explore new opportunities.

Location

Delhi

Work experience

Clinical Research Coordinator at University College of Medical Sciences and GTB Hospital, Nov 2025 - Present · 7 mos, On-site

Intern (Clinical Research Coordinator) at Clinical Research Network India, Mar 2025 - Jun 2025 · 4 mos, Noida, Uttar Pradesh, India, - Conducted participant screening using protocol-defined clinical criteria - Obtained informed consent and maintain enrollment records - Prepared and organized study-specific source documents - Accurately entered source data into the Electronic Data Capture (EDC) system - Coordinated and supported monitoring visits and resolved data queries - Scheduled participant visits and managed study follow-ups - Track, assess, and report adverse events (AEs/SAEs) promptly

Education

Master of Science - MS, Clinical Research, Swami Rama Himalayan University

Vedika Rawat - Clinical Research Coordinator in Delhi | Tal