Clinical Research Coordinator 224410

3 weeks ago


Sacramento, United States Medix™ Full time

Responsibilities:

  • Coordinate daily activities for clinical trials and ensure smooth operation.
  • Administer sponsor-required surveys.
  • Collaborate with colleagues to manage study supplies.
  • Train staff on study procedures and keep records of training.
  • Create and maintain trial documents.
  • Attend meetings as requested.
  • Understand and review study protocols.
  • Assist in recruiting eligible participants.
  • Screen participants based on study criteria.
  • Complete assigned study tasks efficiently.
  • Document and report medical updates and adverse events.
  • Conduct informed consent discussions with participants.
  • Ensure proper implementation of consent forms.
  • Provide oversight in the consent process.
  • Collect and enter data into the system.
  • Ensure data accuracy and resolve queries.
  • Report all adverse events promptly.
  • Coordinate site visits and assist with documentation.
  • Manage regulatory information for the study.
  • Obtain necessary sponsor training and certifications.


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