Clinical Research Coordinator I — Patient-Focused Trials

ObjectiveHealth; Amarillo (TX); On-site; USD 52,000 - 70,000; Full time

Benefits offered by this job

401(k) with Company match

Health insurance

Paid Holidays

Job summary

ObjectiveHealth is seeking a Clinical Research Coordinator I in Texas to manage patient interactions, consent, and study visits. You will work under IRB guidelines to screen, enroll, and monitor participants while ensuring data accuracy and compliance.

The role requires hands-on patient care including blood draws and ECGs, with strong collaboration between the research team and sponsors. Join a mission-driven company advancing clinical trials.

Qualifications

• Experience with IRB approved protocols and patient enrollment.
• Ability to perform blood draws, ECG, and general patient care.
• Strong data entry accuracy and regulatory compliance.

Responsibilities

• Lead patient identification, screening, randomization, and enrollment.
• Conduct clinic visits and direct patient care activities.
• Coordinate with PIs, Sponsors and Monitors.
• Maintain eSource materials and document audit findings.

Skills

Patient care

IRB processes

Data entry

Regulatory compliance

Education

Certified Clinical Research Coordinator

Tools

eSource systems

Job description

ObjectiveHealth is seeking a Clinical Research Coordinator I in Texas to manage patient interactions, consent, and study visits. You will work under IRB guidelines to screen, enroll, and monitor participants while ensuring data accuracy and compliance.

The role requires hands-on patient care including blood draws and ECGs, with strong collaboration between the research team and sponsors. Join a mission-driven company advancing clinical trials.