Clinical Research Coordinator I - Patient-Focused Trials

Objective; St. Louis (MO); On-site; USD 52,000 - 70,000; Full time

Benefits offered by this job

401(k) with Company match

Health, Dental and Vision insurance

PTO

Adoption Assistance

Paid Holidays

Job summary

ObjectiveHealth is seeking a Clinical Research Coordinator I to support patient-focused clinical trials. You will identify, screen, enroll, and monitor patients under IRB-approved protocols and perform direct patient care activities including consent, blood draws, and ECGs.

The role emphasizes precise data entry, regulatory compliance, and strong collaboration with the research team, PIs, sponsors, and monitors to ensure trial quality and patient safety.

Qualifications

• Certification such as an MA or phlebotomy credential is preferred.
• Experience with direct patient care and clinical trial processes is desirable.
• Strong attention to data accuracy, regulatory compliance, and study coordination.

Responsibilities

• Identify, screen, randomize, and enroll patients for IRB approved trials.
• Conduct clinic visits and direct patient care activities (consenting, blood draws, ECG, etc.).
• Maintain accurate eSource data and regulatory documentation.
• Coordinate with the research team, PI, sponsors, and monitors to ensure protocol adherence.

Skills

Patient care

Data entry

Regulatory compliance

IRB protocols

Blood draws

ECG

Documentation

Education

MA certification

Phlebotomy certification

Job description

ObjectiveHealth is seeking a Clinical Research Coordinator I to support patient-focused clinical trials. You will identify, screen, enroll, and monitor patients under IRB-approved protocols and perform direct patient care activities including consent, blood draws, and ECGs.

The role emphasizes precise data entry, regulatory compliance, and strong collaboration with the research team, PIs, sponsors, and monitors to ensure trial quality and patient safety.