Clinical Research Coordinator

1 week ago


Columbia, Missouri, United States Medix™ Full time
Job Summary

We are seeking a highly organized and detail-oriented Clinical Research Assistant to support our research team at Medix®. The successful candidate will play a key role in ensuring the smooth execution of clinical trials, working closely with our Clinical Research Coordinator to coordinate subject visits, prepare documentation, and collect data.

Key Responsibilities
  • Subject Visit Coordination

Schedule and coordinate subject visits according to protocol guidelines and study-specific windows.

Documentation and Data Collection

Prepare visit-related documentation and charts for the Clinical Research Coordinator, and collect and record necessary data for follow-up during study visits.

Support to Clinical Research Coordinator

Observe and support the Coordinator in patient care and management, and assist in monitoring subject flow and providing care.

Administrative Tasks

Transcribe study information from source documents to Electronic Case Report Forms, administer questionnaires to study subjects, and perform other duties as assigned.

Requirements

To be successful in this role, you will need excellent organizational skills, attention to detail, and the ability to work effectively in a team environment. You will also need to be proficient in data collection and management, and have strong communication skills.

We offer a competitive salary and benefits package, as well as opportunities for professional growth and development.



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