Vaishnavi Yeshirao

Thane

Professional Summary

Detail-oriented Clinical Data Management professional with 1.5 years of hands-on experience coordinating clinical research activities under the ICMR. Skilled in managing eCRFs, ensuring data accuracy, and supporting clinical trial studies. Strong analytical thinker with proficiency in data tools like Castor EDC and Power BI. Passionate about driving impactful insights in clinical research through meticulous data evaluation and cross-functional collaboration.

Key Skills

• Clinical Data Management (CDM)
• Data Cleaning & Validation
• Castor EDC | Veeva Vault Basics
• eCRFs | ICH-GCP | 21 CFR Compliance
• Power BI | Intermediate R Programming
• Clinical Trials & Regulatory Affairs
• Onsite Monitoring & Enrollment Oversight
• Strong Analytical & Communication Skills
• Communication with Sponsors

Certifications

• Principles and Practice of Clinical Research – NIH
• Good Clinical Practice – NIDA
• Clinical Data Management – Biotecnika
• Regulatory Affairs (Udemy) & EU MDR (Mini-Course)

Professional Experience

Project Technical Support III (ICMR-Adhoc)

LTMMC | Mumbai

March 2023 – September 2024

• Collaborated with research teams to manage and analyze clinical data.
• Maintained accuracy and integrity of datasets across trial lifecycle
• Led site-level clinical trial management including data compilation, eCRFs, and patient follow-up tracking
• Supported IRB/IEC ethical submissions and liaised with sponsors for data communication and compliance
• Achieved 90%+ follow-up compliance on 100+ patient enrollments through proactive engagement and data oversight

Education

• M.Sc. Microbiology – HBSU, Mumbai (2020 – 2022)
• B.Sc. Microbiology – University of Mumbai (2017 – 2020)

Languages

English | Hindi | Marathi

Keywords: Clinical Data Management, Data Cleaning & Validation, Castor EDC, eCRFs, Power BI, Clinical Trials, Regulatory Affairs, Analytical Skills, Communication Skills

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Cover Letter:

I am dedicated and enthusiastic to work in clinical research and have experience in clinical trial operations and regulatory guidelines
Given the chance I adapt to fast-paced roles and being tech savvy gives me an edge.