Clinical Research Coordinator: Lead Trials & Data

Folio Clinical Research; Murrieta (CA); On-site; USD 36,000 - 50,000; Full time

Job summary

Folio Clinical Research in Murrieta, CA is hiring a Clinical Research Coordinator to support conduct of clinical trials. You will assist with lab processing, data entry, recruitment, and scheduling, collaborating with investigators, site staff, and sponsors to ensure timely study execution.

The role requires attention to detail, strong communication, and adherence to GCP/IRB guidelines, with opportunities to work across multiple studies and technologies.

Qualifications

• Bachelor’s degree in science/health field required.
• 1+ year CRC experience or 2+ years CRA experience.
• Experience with EDC, CTMS and eTMF systems.
• Knowledge of ICH-GCP and regulatory requirements.
• Experience in data management and data integrity.
• Strong communication skills, written and verbal.

Responsibilities

• Assist PI/SI and other CRCs with lab processing, data entry, and subject pre-screening, recruitment, and scheduling.
• May lead several studies from qualification to close-out as primary resource.
• Set up site, calibrate equipment, and order necessary supplies.
• Attend SQVs, SIVs, and monitoring visits with PI/SI and prepare FPV/FPS/FPE.
• Support CRCs, Clinical Research Assistants, and Regional Managers to grow the program.
• Assist with unblinded study responsibilities without breaking blinding.

Skills

Interpersonal communication

Attention to detail

Time management

Multitasking

Computer skills

Education

Bachelor’s degree in science/health

Phlebotomy experience preferred

Tools

CTMS

eTMF

EDC

IXRS

RTSM

MS Office

Job description

Folio Clinical Research in Murrieta, CA is hiring a Clinical Research Coordinator to support conduct of clinical trials. You will assist with lab processing, data entry, recruitment, and scheduling, collaborating with investigators, site staff, and sponsors to ensure timely study execution.

The role requires attention to detail, strong communication, and adherence to GCP/IRB guidelines, with opportunities to work across multiple studies and technologies.