Carylle Panaligan

About Carylle

I’m a hardworking and detail-oriented professional with 5 years of experience in clinical research data entry. My duties include entering clinical trial data from source documents into electronic data capture (EDC) systems, checking records for accuracy and completeness, and resolving data discrepancies with the research team. I also maintain study documents and participant records, assist with data cleaning and quality checks before database lock, and prepare study reports when needed. I make sure to follow study protocols, Good Clinical Practice (GCP), and data privacy requirements. I’m used to handling a high volume of records, meeting deadlines, and working independently. I’m now looking for a remote opportunity where I can use my experience and continue to grow professionally.

Skills

Experience

• I have 5 years of experience in clinical research data entry, handling patient records, checking information for accuracy, and maintaining study documents.
• I have experience working with databases, electronic data entry systems, and Microsoft Office tools.
• One of my strengths is handling a high volume of records while staying organized and paying attention to detail.
• I’m comfortable learning new tools, working independently, and meeting daily targets.
• I’m also open to different work schedules, including night shifts and shifting schedules, depending on the role.