Clinical Research Coordinator II - Patient-Centric Trials

ObjectiveHealth; St. Louis (MO); On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

401(k) with company match

Health insurance

Paid Holidays

Disability benefits

PTO

Job summary

ObjectiveHealth is seeking a Clinical Research Coordinator II to join our patient-centered research team in a full-time capacity. The ideal candidate will manage IRB-approved protocols, screen and enroll patients, and coordinate clinic visits with meticulous attention to data quality.

You will work closely with physicians, sponsors, and monitors to ensure compliance, accurate documentation, and timely study startup and maintenance.

Qualifications

• 3+ years of clinical research coordination experience.
• Experience with IRB approved protocols, patient enrollment, and clinic visits.

Responsibilities

• Identify, screen, randomize and enroll patients in IRB-approved protocols.
• Conduct clinic visits and perform direct patient care activities (consenting, assessments, blood draws, ECG).
• Maintain clean data entry, regulatory compliance, and audit-ready study documentation.
• Coordinate study setup and maintenance across sites with PI, sponsors and monitors.

Skills

IRB protocol

Consent patients

Patient care

Data entry

Regulatory compliance

Study coordination

Job description

ObjectiveHealth is seeking a Clinical Research Coordinator II to join our patient-centered research team in a full-time capacity. The ideal candidate will manage IRB-approved protocols, screen and enroll patients, and coordinate clinic visits with meticulous attention to data quality.

You will work closely with physicians, sponsors, and monitors to ensure compliance, accurate documentation, and timely study startup and maintenance.