Clinical Research Coordinator - Day Shift, Impactful Trials

adventhealth; Calhoun (GA); On-site; USD 43,000 - 80,000; Full time

Job summary

AdventHealth in Calhoun, GA is seeking a Clinical Research Coordinator to oversee end-to-end clinical research activities, including patient screening, enrollment, and follow-up care in a fast-paced environment. You will serve as the primary liaison for participants, investigators, and research partners while ensuring adherence to AHRI protocols.

The role requires coordinating biospecimen collection, maintaining HIPAA-compliant databases, and supporting operations through data collection and

Qualifications

• Bachelor's degree in healthcare or related field required.
• Master's degree preferred.
• 2+ years direct clinical research or data-related experience preferred.
• Certified Clinical Research Coordinator or SOCRA/CCRP certification preferred.

Responsibilities

• Manage end-to-end clinical research activities, including patient screening, eligibility, enrollment, and follow-up care.
• Serve as the primary liaison for participants, investigators, and internal/external research partners.
• Ensure compliance with clinical research standards, protocols, and AHRI procedures across all patient-facing activities.
• Coordinate biospecimen collection and maintain HIPAA-compliant databases linking patient data to research samples.
• Support research operations through data collection, chart review, and collaboration with clinical, lab, and regulatory teams.

Skills

HIPAA compliance

Communication

Analytical thinking

Attention to detail

Organization & multitasking

Microsoft Office

EDC exposure

Clinical research knowledge

Research coordination

Interpersonal skills

Education

Bachelor's degree

Master's degree

Tools

CTMS

Electronic Data Capture (EDC)

Job description

AdventHealth in Calhoun, GA is seeking a Clinical Research Coordinator to oversee end-to-end clinical research activities, including patient screening, enrollment, and follow-up care in a fast-paced environment. You will serve as the primary liaison for participants, investigators, and research partners while ensuring adherence to AHRI protocols.

The role requires coordinating biospecimen collection, maintaining HIPAA-compliant databases, and supporting operations through data collection and