A company is looking for a PS Study Coordinator to manage clinical research studies within the Gastroenterology and Hepatology division.
Key Responsibilities
Coordinate patient recruitment, screening, and enrollment for clinical research studies
Ensure timely and accurate collection of patient samples and monitor patient safety
Maintain compliance with FDA guidelines and prepare necessary documentation for studies
Required Qualifications
Bachelor's degree in a related field or equivalent experience
Certification in the Protection of Human Research Subjects within six months of hire
Ability to meet vaccination requirements for patient-sensitive roles
Demonstrated potential to perform essential job functions
Some departments may require additional training within six months
Clinical Research Coordinator • Irving, Texas, United States
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