Patient-Centered Clinical Research Coordinator I

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

Benefits offered by this job

401(k) with Company match

Health, Dental and Vision insurance

Paid Holidays

Generous PTO

Adoption Assistance

Job summary

ObjectiveHealth is seeking a Clinical Research Coordinator I to support IRB-approved trials, screen and enroll patients, and perform direct patient care tasks such as blood draws and ECGs. The role emphasizes data integrity, regulatory compliance, and collaboration with investigators and sponsors.

The ideal candidate will have MA or phlebotomy certification and a strong commitment to patient-centered research across Gastroenterology, Urology, Dermatology, and Oncology studies.

Qualifications

• Certification such as MA or phlebotomy.
• Experience with IRB-approved clinical trial protocols: screening, randomization, enrollment.
• Direct patient care activities: consenting patients, blood draws, ECG, medication administration.

Responsibilities

• Identify, screen, randomize, and enroll patients.
• Conduct clinic visits and provide direct patient care.
• Maintain regulatory documentation and eSource materials; track AE/SAE and audit findings.
• Coordinate with study team, PIs, Sponsors, and monitors.

Skills

Patient interaction

Clinical trial procedures

Communication

Data entry accuracy

Regulatory compliance

IRB protocol knowledge

Education

MA or phlebotomy certification

Tools

eSource systems

Job description

ObjectiveHealth is seeking a Clinical Research Coordinator I to support IRB-approved trials, screen and enroll patients, and perform direct patient care tasks such as blood draws and ECGs. The role emphasizes data integrity, regulatory compliance, and collaboration with investigators and sponsors.

The ideal candidate will have MA or phlebotomy certification and a strong commitment to patient-centered research across Gastroenterology, Urology, Dermatology, and Oncology studies.