Care-Driven Clinical Research Coordinator I

ObjectiveGI, Inc.; Columbia Township (MO); On-site; USD 48,000 - 64,000; Full time

Benefits offered by this job

Competitive pay

401(k) match

Career progression

Disability insurance

Health Savings Account

Health/dental/vision insurance

Paid time off

Adoption assistance

Paid holidays

Job summary

ObjectiveHealth in Missouri is seeking a Clinical Research Coordinator I to support patient-focused trials. You will identify, screen, enroll and follow patients under IRB-approved protocols, conduct clinic visits, and assist with data collection and regulatory tasks.

The ideal candidate holds a certification such as MA or phlebotomy, enjoys direct patient interaction, and can manage multiple studies with attention to detail to ensure protocol adherence and accurate documentation.

Qualifications

• Certification such as MA or phlebotomy preferred.
• Experience with IRB-approved clinical trial protocols and regulatory processes.
• Strong patient-care and patient-interaction skills.

Responsibilities

• Identify, screen, randomize, and enroll patients per protocol.
• Conduct clinic visits and direct patient care activities (consenting, assessments, blood draws, ECG).
• Maintain data integrity and regulatory compliance; manage eSource and study setup.

Skills

Patient interaction

IRB protocols

Screening & enrollment

Clinic visits

Data entry & accuracy

Regulatory compliance

Study coordination

Communication

Job description

ObjectiveHealth in Missouri is seeking a Clinical Research Coordinator I to support patient-focused trials. You will identify, screen, enroll and follow patients under IRB-approved protocols, conduct clinic visits, and assist with data collection and regulatory tasks.

The ideal candidate holds a certification such as MA or phlebotomy, enjoys direct patient interaction, and can manage multiple studies with attention to detail to ensure protocol adherence and accurate documentation.