Clinical Research Coordinator I — Patient-Focused Trials

ALLIANCE CLINICAL LLC; Los Angeles (CA); On-site; USD 34,000 - 44,000; Full time

Benefits offered by this job

Medical

Dental

Vision

401k

PTO

and more!

Job summary

Alliance Clinical Network is seeking a Clinical Research Coordinator I to support clinical trials at our West Hills and Canoga Park sites. The role covers coordinating visits, data capture, and regulatory compliance with GCP guidelines, while ensuring participant safety and protocol fidelity.

The Coordinator will conduct health assessments, obtain informed consent, manage IP documentation, and assist with site start-up and monitoring activities in a fast-paced setting.

Qualifications

• Requires CPT license and 2+ years phlebotomy/EKG experience.
• Associate degree or equivalent in healthcare or related field.
• Minimum 2 years in healthcare setting; knowledge of FDA regulations and GCP.

Responsibilities

• Coordinate study visits and data collection per protocol.
• Maintain regulatory files and conduct source data verification.
• Obtain informed consent and ensure participant safety and privacy.
• Assist with adverse event reporting and safety monitoring.
• Support study startup, timelines, and collaboration with the PI.

Skills

Phlebotomy

EKG procedures

Attention to detail

Communication

Education

Associate's degree in healthcare or related field

CPT license (Certified Phlebotomy Technician)

Job description

Alliance Clinical Network is seeking a Clinical Research Coordinator I to support clinical trials at our West Hills and Canoga Park sites. The role covers coordinating visits, data capture, and regulatory compliance with GCP guidelines, while ensuring participant safety and protocol fidelity.

The Coordinator will conduct health assessments, obtain informed consent, manage IP documentation, and assist with site start-up and monitoring activities in a fast-paced setting.