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Clinical Trial Data Coordinator I
ICON
hybrid
Warsaw, Poland
About this role
Clinical Trial Data Coordinator I
ICON
What you will be doing
- Review clinical trial data captured in electronic data capture systems
- Identify missing, inconsistent, or out-of-range data
- Generate, track, and resolve data queries
- Ensure data aligns with study protocols and data management plans.
- Perform ongoing data quality checks and trend reviews.
Your profile
- Master’s degree in a relevant field (e.g., Life Sciences or Healthcare, Biology, Pharmacy, etc), candidates in the final stage of their Master’s studies can also be considered.
- Availability to commence work on 2nd November
- Able to work in a hybrid setup: 3 days per week on-site at the client’s office in Warsaw
- Fluent English
- Basic knowledge of clinical data management within the pharmaceutical or biotechnology industry.
- Familiarity with data management software and systems
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