Clinical Research Data Coordinator 240873 Job at Medix™, East Brunswick, NJ

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  • Medix™
  • East Brunswick, NJ

Job Description

Data Management:

  • Collect and manage clinical trial data from different sources, like forms and electronic systems.
  • Make sure the data is accurate, complete, and entered on time.
  • Check for errors or mismatches in the data and work with the research team to fix them.
  • Help get the data ready for analysis.

Study Documentation:

  • Keep study files organized and up-to-date, following all rules and regulations.
  • Make sure all required documents, like consent forms and approvals, are current and ready for audits.
  • Track important dates and deadlines for the study.

Compliance & Quality Control:

  • Review data to make sure it follows study rules and Good Clinical Practice (GCP) guidelines.
  • Help prepare for visits and audits from regulatory agencies.
  • Ensure the study meets all legal, ethical, and privacy standards.

Collaboration & Communication:

  • Work with investigators, coordinators, and other team members to support the study.
  • Communicate with outside groups like sponsors, CROs, and regulators to keep data flowing smoothly.
  • Create regular updates on how the study is going, including any issues with the data.

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