I am an experienced clinical research coordinator who is medical professional ( 8 years of hands on clinical experience) from India. Experienced Clinical Research Coordinator (CRC) that handles regulatory, entirety of visit (including blood draw) and communicating with the PI/Subl for each study every day.I am passionate to use my prior medical/clinical knowledge in the field of clinical research with training and experience of ICH-GCP E6 and 21 CFR part 11, 50, 54 and 56. I have experience in SSV and IMV also comfortable maintaining a regulatory binder. I am proficient in GCP following ALCOA-C principles in coordinating clinical trials ethically and of scientific quality. I have proven skills as a good administrator and a clinical coordinator who has interacted with different specialty physicians in the hospital in a healthy working environment. Well organized, structured, punctual and passionate individual with exceptional multitasking abilities.- Performed quality assurance checks on more than200 active study participant charts for data accuracy and source completion in preparation for FDA audit for Moderna pediatric study and booster study extension. Streamlined discrepancy findings into a distributable spreadsheet for team member corrections.- Also, regularly performed QA/QC duties in between 3 separate sites for many different studies within private practices successfully and efficiently.-Experience with Clinical Conductor, iMedidata, inform oracle, endpoint, trialmax, impala for Pfizer, preclarus, ePip, green fire, Florence, SBIR, and eClinicalWorks, among other CTMSand EMR platforms.