Clinical Research Coordinator II — Patient Care & Trials Lead

ObjectiveGI, Inc.; St. Louis (MO); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

401(k) with Company match

Health, Dental and Vision insurance

Generous PTO

Adoption Assistance

Paid Holidays

Disability insurance

Job summary

ObjectiveHealth is hiring a Clinical Research Coordinator II in Missouri to support patient-focused trials. You will coordinate screenings, enroll patients, conduct clinic visits, collect data, and ensure regulatory compliance.

This full-time role requires 3+ years of experience and a collaborative, detail-oriented approach. You will work closely with investigators, sponsors, and monitors to meet enrollment targets and maintain high-quality data.

Qualifications

• 3+ years of clinical research coordination experience.
• Experience with IRB approved protocols and patient consent.
• Ability to perform clinic visits, blood draws, ECG and data entry.

Responsibilities

• Coordinate and manage IRB-approved clinical trials across sites.
• Screen, enroll and follow patients per protocol; obtain consent.
• Ensure regulatory compliance and accurate data entry.

Skills

Patient interaction

Team player

Attention to detail

Regulatory compliance

IRB protocols

Data entry

Communication

Job description

ObjectiveHealth is hiring a Clinical Research Coordinator II in Missouri to support patient-focused trials. You will coordinate screenings, enroll patients, conduct clinic visits, collect data, and ensure regulatory compliance.

This full-time role requires 3+ years of experience and a collaborative, detail-oriented approach. You will work closely with investigators, sponsors, and monitors to meet enrollment targets and maintain high-quality data.