Clinical Research Coordinator

Duties

• Covers administrative tasks such as coordinating with Principal Investigator, local site, and Central Hub.
• Aids in developing materials and tools for training study participants and team members.
• Prepares and reviews regulatory submission documents.
• Organizes and establishes study files.
• Understands and communicates study requirements to all involved parties.
• Communicates with research participants during the informed consent process.
• Screens potential participants for eligibility.
• Registers participants in CTMS for billing purposes.
• Coordinates participant tests and procedures.
• Maintains study timelines and inventory of study supplies.
• Completes and maintains study documentation.
• Communicates with sponsor and research participants during the study.
• Manages day-to-day activities of the study including problem-solving and protocol management.
• Assists in submitting accurate and timely closeout documents.

Requirements

• Preferred clinical research experience.
• Previous phlebotomy skills.
• High School Diploma.

Benefits

• Growth opportunities within the rapidly expanding team.
• Competitive compensation.
• Comprehensive benefits package.

Pay

Competitive compensation.

Schedule

No weekends or evenings – Monday through Friday.

Benefits

• Paid holidays and paid time off.
• Retained study documents according to Gastro Health Research policy or for the contracted length of time, whichever is longer.