Dynamic Clinical ResearchCoordinator – Denver Trials

Green Life Science; Denver (CO); Hybrid; USD 65,000 - 90,000; Full time

Benefits offered by this job

Competitive salary

Professional development opportunities

Long-term career growth

Job summary

Green Life Science is seeking a Clinical Research Coordinator in Denver, Colorado to join a fast-paced, patient-facing research environment. You will coordinate studies from start-up through close-out across a diverse portfolio, ensuring data quality, patient care and regulatory compliance.

The ideal candidate will have hands-on experience with GCP, FDA regulations, vital signs, ECGs, phlebotomy and source documentation, plus strong communication and attention to detail to support recruitment

Qualifications

• Minimum experience as a CRC in a clinical research site.
• Strong knowledge of GCP and FDA regulations.
• Experience supporting patient recruitment and retention.

Responsibilities

• Coordinate clinical research studies in accordance with protocols, GCP and applicable regulations.
• Conduct patient-facing study visits including screening, enrollment, follow-up and end-of-study visits.
• Support patient recruitment, prescreening, scheduling and retention activities.
• Perform and document clinical procedures including: vital signs, 12-lead ECGs, phlebotomy and specimen processing.
• Maintain accurate source documentation and study records; complete EDC entries and respond to data queries.

Skills

GCP knowledge

Clinical trial coordination

Communication

Attention to detail

Independent work

Education

Bachelor's degree in life sciences

Tools

EDC systems

Job description

Green Life Science is seeking a Clinical Research Coordinator in Denver, Colorado to join a fast-paced, patient-facing research environment. You will coordinate studies from start-up through close-out across a diverse portfolio, ensuring data quality, patient care and regulatory compliance.

The ideal candidate will have hands-on experience with GCP, FDA regulations, vital signs, ECGs, phlebotomy and source documentation, plus strong communication and attention to detail to support recruitment