Clinical Research Coordinator II — Patient-Focused Trials

ObjectiveHealth; Columbia Township (MO); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

401(k) plan

Health, Dental, Vision

Paid time off

Adoption assistance

FSA benefits

Job summary

ObjectiveHealth in the United States seeks a Clinical Research Coordinator II to join our patient-centered team. You will coordinate IRB-approved protocols, screen and enroll patients, and manage patient visits while ensuring accurate data collection.

The ideal candidate has 3+ years of clinical research coordination experience, strong communication, and a diligent eye for detail to support investigators, sponsors, and monitors, upholding regulatory compliance and patient safety.

Qualifications

• 3+ years of clinical research coordination experience.
• Experience with IRB approved protocols.
• Experience with patient consenting, visits, and data collection.

Responsibilities

• Own assigned studies and patient visits.
• Coordinate screening, enrollment, and follow-up per protocol.
• Ensure regulatory compliance and accurate data entry.
• Collaborate with investigators, sponsors, monitors.

Job description

ObjectiveHealth in the United States seeks a Clinical Research Coordinator II to join our patient-centered team. You will coordinate IRB-approved protocols, screen and enroll patients, and manage patient visits while ensuring accurate data collection.

The ideal candidate has 3+ years of clinical research coordination experience, strong communication, and a diligent eye for detail to support investigators, sponsors, and monitors, upholding regulatory compliance and patient safety.