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Clinical Trial Operations Specialist
1 week ago
iSupport Worldwide is a leading provider of medical coding services for clinical trials.
We are committed to delivering high-quality services to our clients and strive to build long-term relationships with them.
We offer a comprehensive benefits package, professional development opportunities, and a collaborative work environment.
If you are a motivated and detail-oriented individual who is passionate about medical coding, we encourage you to apply for this exciting opportunity.
Responsibilities- Clinical Data Collection: Collect clinical data from medical records, research charts, and other source documents.
- Data Analysis: Analyze collected data to identify trends and patterns.
- Study Protocol Compliance: Ensure that all data is compliant with study protocols.
- Collaboration: Collaborate with the research team to ensure seamless project execution.