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Clinical Research Data Specialist

1 week ago

Manila, National Capital Region, Philippines iSupport Worldwide Full time
About the Role

At iSupport Worldwide, we are seeking a skilled Clinical Trial Medical Coder to join our research team. The successful candidate will be responsible for collecting and abstracting clinical data from medical records, research charts, and other source documents.

This role involves performing data integrity and quality checks on entered data, source document verification, and ensuring compliance with study protocols.

The position also includes managing patient follow-up for maintained registries and trials, overseeing data management, adherence reporting, and compliance documentation.

We require a strong understanding of healthcare operations and excellent analytical skills to make informed decisions.

Key Responsibilities
  • Data Collection and Abstracting: Collect and abstract clinical data from medical records, research charts, and other source documents.
  • Data Integrity and Quality Checks: Perform data integrity and quality checks on entered data to ensure accuracy and completeness.
  • Source Document Verification: Verify source documents to ensure compliance with study protocols.
  • Patient Follow-Up: Manage patient follow-up for maintained registries and trials.
  • Data Management: Oversee data management, including data entry, data cleaning, and data analysis.