Patient-Focused Clinical Research Coordinator II

ObjectiveHealth; South Carolina; On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

401(k) with Company match

Health, Dental and Vision insurance

Generous PTO

Adoption Assistance

Paid Holidays

Health Savings and Flexible Spending

Job summary

ObjectiveHealth in the United States is seeking a Clinical Research Coordinator II to manage IRB-approved studies, screen and enroll patients, and coordinate clinic visits across specialty areas. A minimum of 3+ years in clinical research coordination is required and patient-facing experience is essential.

You will ensure data integrity, regulatory compliance, and direct patient care while collaborating with investigators, sponsors, and monitors.

Qualifications

• 3+ years of clinical research coordination experience.
• Experience conducting IRB-approved trials, patient screening, enrollment, and clinic visits.
• Ability to consent patients and perform basic clinical procedures.
• Strong data entry accuracy and regulatory compliance.

Responsibilities

• Own assigned studies and patients.
• Coordinate visits, data collection, and regulatory documentation.
• Communicate effectively with leadership and study team.
• Maintain protocol adherence and timely IRB responses.

Skills

Patient interaction

Team player

Attention to detail

Regulatory compliance

Clear communication

IRB protocol experience

Job description

ObjectiveHealth in the United States is seeking a Clinical Research Coordinator II to manage IRB-approved studies, screen and enroll patients, and coordinate clinic visits across specialty areas. A minimum of 3+ years in clinical research coordination is required and patient-facing experience is essential.

You will ensure data integrity, regulatory compliance, and direct patient care while collaborating with investigators, sponsors, and monitors.