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Ritika Nayan

Ritika Nayan

  • Screen potential study participants
  • Performs informed consent of participants.
  • Completes, audits, and corrects CRFs.
  • Reviews and ensures adherence to study protocol.
  • Maintain complete records of research study activities.
  • Transmission of clinical case data to the data management centers.
  • Reviews and responds to case report form queries.