New Delhi, India
Clinical Research Associate | Clinical Trial Support | Data Entry | Ex
Local Time - 09:41 PM
About Me
I am a dedicated Clinical Research Associate with 5 years of experience in clinical trials, site monitoring, and regulatory documentation. I have worked extensively with CROs, sponsors, and investigator sites, ensuring accurate data entry, GCP compliance, and smooth trial execution.
Alongside my CRA work, I specialize in creating and managing Trial Master Files TMF, site tracking logs, visit reports, and data entry in Excel or EDC systems. I also help teams with clean and well formatted Microsoft Word and Excel documents.
I am punctual, reliable, and detail oriented — always focused on delivering high quality work within deadlines.
My Expertise
Clinical Trial Documents Logs, CV Tracker, TMF Checklists
Data Entry Excel, eCRF, EDC tools like Oracle, Octalsoft, etc.
Monitoring Visit Reports PSV, SIV, IMV, COV
MS Excel Reporting and Formatting
SOP Writing and Document Templates
PowerPoint Presentation Editing
My Expertise
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$5/hr
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