What are the responsibilities and job description for the Clinical Research Coordinator position at Apex Cardiology?
Job Overview
The Clinical Research Coordinator supports clinical trials from study start-up through closeout, helping protect participant safety and maintain reliable, compliant research data. This role works with investigators, participants, clinical teams, and laboratory staff in a research setting. Your impact: Careful participant monitoring and accurate data collection help research teams make informed decisions while supporting participant safety.
Duties
- Coordinate clinical trials, study schedules, documentation, and research project management activities in line with protocols and clinical research methods.
- Monitor participants, collect vital signs and blood samples as assigned, and document study activities in electronic medical record (EMR) systems.
- Review study records and manage data using appropriate data management practices, statistical software, and Microsoft Office.
- Support clinical research compliance, healthcare compliance, compliance management, and clinical quality assurance standards, including applicable Food and Drug Administration (FDA) regulations, International Council for Harmonisation (ICH) guidelines, Good Clinical Practice (GCP), ethical guidelines, and Health Insurance Portability and Accountability Act (HIPAA) requirements.
- Coordinate with clinical laboratory teams and contribute to clinical development activities while following applicable Clinical Data Interchange Standards Consortium (CDISC) standards.
Experience
- Experience in clinical research, clinical trials management, research, or a related research setting; clinical laboratory experience is required.
- Knowledge of medical terminology, patient monitoring, documentation review, data collection, and analysis skills.
- Project management experience, particularly in healthcare or research project management, is required; supervising experience is an asset.
- Familiarity with clinical research methods, clinical research compliance, and relevant ethical and quality standards is expected.
- An ICH Good Clinical Practice (GCP) certificate from any valid issuer for California is preferred.
Pay: $17.00 - $25.00 per hour
Expected hours: 40.0 per week
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Health insurance
- Life insurance
- Retirement plan
- Vision insurance
Work Location: In person
Salary : $17 - $25