Clinical Research Coordinator II: Impactful, Patient-Centered Trials

ObjectiveGI, Inc.; Columbia Township (MO); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

401(k) with company match

Health Savings Account & Flexible StIP

Health, Dental and Vision insurance

Generous PTO

Adoption Assistance

Paid Holidays

Job summary

ObjectiveHealth is seeking a Clinical Research Coordinator II in Missouri to support multiple GI, urology, dermatology and oncology trials. You will manage patient consent, scheduling and data entry, ensuring protocol adherence and regulatory compliance in a fast-paced clinical setting.

The role emphasizes accurate documentation, collaboration with PIs, sponsors and monitors, and delivering high-quality enrollment metrics across diverse studies.

Qualifications

• 3+ years of clinical research coordination experience.
• Experience with IRB approved protocols and regulatory requirements.
• Strong patient interaction and data-entry accuracy.

Responsibilities

• Identify, screen, randomize and enroll patients per protocol.
• Conduct clinic visits and direct patient care activities (consenting, assessments, blood draws, ECG).
• Maintain regulatory compliance and clean data entry across the study.

Skills

Clinical research coordination

Job description

ObjectiveHealth is seeking a Clinical Research Coordinator II in Missouri to support multiple GI, urology, dermatology and oncology trials. You will manage patient consent, scheduling and data entry, ensuring protocol adherence and regulatory compliance in a fast-paced clinical setting.

The role emphasizes accurate documentation, collaboration with PIs, sponsors and monitors, and delivering high-quality enrollment metrics across diverse studies.