Clinical Research Coordinator: Patient-Centric Trials

Green Life Science; Charlotte (NC); On-site; USD 55,000 - 75,000; Full time

Job summary

Green Life Science in Charlotte, NC is seeking a Clinical Research Coordinator to join our patient-focused clinical trials team. You will manage start-up through study completion, coordinating visits, obtaining informed consent, and maintaining source documentation and data entry in EDC/EMR systems.

Responsibilities include recruiting and screening participants, conducting study visits, monitoring safety, and ensuring compliance with ICH-GCP and SOPs.

Qualifications

• Experience as CRC or in a clinical research site.
• Experience supporting patient visits, recruitment, screening and study documentation.
• Knowledge of ICH-GCP, trial protocols and regulatory requirements.
• Strong organisational skills with multiple studies and priorities.
• Excellent communication and patient-facing skills.
• Experience with EDC and EMR preferred.
• Phlebotomy, ECG and other clinical assessment experience advantageous.

Responsibilities

• Coordinate studies from start-up through completion following protocols and regulatory requirements.
• Recruit, screen and schedule participants for trials.
• Conduct informed consent discussions and document findings.
• Perform study visits, patient assessments, vitals, ECGs and samples as required.
• Maintain source docs, case report forms and data entry in EDC/EMR.
• Monitor participant safety and document adverse events.
• Collaborate with investigators, nurses and site staff for efficient delivery.
• Ensure compliance with GCP, SOPs and regulatory guidelines.

Skills

Communication skills

Organizational skills

Patient-facing

Team collaboration

Tools

EDC systems

EMR systems

Job description

Green Life Science in Charlotte, NC is seeking a Clinical Research Coordinator to join our patient-focused clinical trials team. You will manage start-up through study completion, coordinating visits, obtaining informed consent, and maintaining source documentation and data entry in EDC/EMR systems.

Responsibilities include recruiting and screening participants, conducting study visits, monitoring safety, and ensuring compliance with ICH-GCP and SOPs.