Mayuri Thorat

Clinical Research Coordinator @Bhaktivedanta Hospital & Research Institute

Mumbai, MH, IN
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Jul 2024 — Present

Clinical Research Coordinator @Bhaktivedanta Hospital & Research Institute

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Thane, IN

Successfully completed a one-year internship in Clinical Trials, gaining hands-on experience in research protocols and regulatory compliance. Coordinated clinical trial activities, ensuring adherence to ICH-GCP guidelines, study protocols, and local regulations. Assisted Principal Investigator (PI) and site study team in meeting sponsor and regulatory requirements. Managed protocol-related procedures, including subject recruitment, scheduling, screening, and enrolment. Performed timely CRF data entry and accurately transcribed source documents under PI supervision. Coordinated ethics committee submissions, ensuring timely documentation and compliance. Prepared patient files and site documentation for site monitoring visits. Maintained and updated the clinical trial management sheet, ensuring accurate inventory tracking. Assisted PI in SAE Reporting on Sugam Portal

EDUCATION

N/A

Bhaktivedanta Hospital and Research Institute

Postgraduate Diploma, Clinical Research Coordinator

N/A

AAKASH INSTITUTE

Science

N/A

A.P International School

School , Science

N/A

Abhinav College of Arts, Commerce & Science

Bachelor of Science - BS, Microbiology and Immunology

ABOUT MAYURI THORAT

Skilled in conducting feasibility assessments, managing site documentation, and ensuring compliance with regulatory and sponsor requirements. Proficient in Good Clinical Practice (GCP), ICH guidelines, and regulatory requirements, with expertise in coordinating study start-up activities, assessing patient recruitment potential, and streamlining trial initiation processes. Adept at liaising with investigators, sponsors, ethics committee and CROs to facilitate efficient study execution. Detail-oriented and highly organized, with excellent problem-solving and communication skills. Committed to maintaining ethical research standards while optimizing clinical trial operations across multiple therapeutic areas.

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