Data/Clinical Research Coordinator



Summary

The Data/Clinical Research Coordinator will particpate in clinical research activities held at Texas Children's Hospital. Job responsibilities include: entering complete, accurate, and timely data entry for clinical research studies including collection and transcription of research patient data and study-related information into case report forms.

Job Duties
  • Assists in completing protocol-specific documents.
  • Utilizes institutional and sponsor databases to record and track enrollment data.
  • Obtains accurate medical information from patient charts.
  • Meets with assigned study coordinator and investigator on a regular basis to review collected data and provide study updates.
  • Maintains logs/progress reports to track current and follow-up participants.
  • Creates study-specific data collection worksheets and Manual of Operations.
  • Prepares for sponsor monitoring visits and responds to sponsor queries.
  • Assists with audits/regulatory inspections and participates in study initiation meetings.
  • Attends sponsor calls and provides pertinent updates to study coordinator and the PI.
  • Registers consented patients and their study visits in RRO Subject Registration System.
  • May participate in consenting patients.
  • Attends team meetings and individual weekly meetings with supervisor.


Minimum Qualifications
  • High School diploma or GED.
  • Two years of relevant experience.


Preferred Qualifications
  • Two years experience.
  • Bachelor degree in a scientific or healthcare related field.
  • SoCRA or ACRP CRA, CRC or CRP certification.
  • Experience with EPIC is a plus.


Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.

6894

CA; CH

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