Vishal Yerekar

• Managed and maintained clinical study documentation, including Study Files, CRFs, and Monitoring Files, ensuring readiness for internal and external audits • Contributed in the coordination and administration of clinical studies from start-up through execution and close-out • Utilized Clinical Trial Management Systems to update and track trial progress, ensuring accurate and timely information for project teams • Conducted quality control audits of clinical study documentation

• Identification, naming and categorizing of all type of documents (Clinical/Non-Clinical/Regulatory) • Conduct quality check of all the documents, rectifying the errors before submitting the work for execution • Resolved query log, conducted update session and sharing the resolution with processor

Interpretation, analysis and organization of clinical trials (ongoing, completed, published) obtained from different sources such as media releases, company/university/Institution sponsored publications, authentic registry sites(e.g. Clinicaltrials.gov, Eudract) with respect to drugs in focus, diseases or conditions for therapy/prophylaxis, other important medical details (trial phase, drug dosages, etc) in a form ready to use for the end-users.