Clinical Research Associate II – Regional Field Monitor

ICON; Washington; On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

LifeWorks EAP

Life assurance

Flexible benefits

Job summary

ICON is seeking a Clinical Research Associate to join the Cross Therapeutic team for the Northwest Region in the United States. You will be the primary liaison between investigational sites and sponsors, perform site visits, ensure ICH-GCP compliance, and maintain CTMS and eTMF documentation to support data quality and patient safety.

The ideal candidate has a Life Sciences degree or an RN, 2+ years of on-site monitoring in pharma/CRO, and travel up to 50%.

Qualifications

• Bachelor’s degree in Life Sciences or equivalent required. RN qualification acceptable.
• 2+ years of on-site monitoring experience in pharma/CRO environment.
• Proficient with ICH-GCP and local regulatory requirements.
• Experience with CTMS and eTMF systems.

Responsibilities

• Serve as primary point of contact between investigational sites and sponsor.
• Conduct site visits (selection, initiation, routine monitoring, close-out).
• Ensure site compliance with ICH-GCP, SOPs and regulations.
• Maintain CTMS and eTMF documentation.
• Support site staff training and compliance records.
• Monitor patient safety and AE/SAE/PQC reporting.
• Support subject recruitment and retention at site level.
• Oversee drug accountability and storage/destruction.
• Resolve data queries and drive timely data entry.
• Document site progress and elevate risks to the clinical team.
• Assist in tracking site budgets and payments.
• Collaborate with CTAs, LTMs, and CTMs.

Skills

Clear communicator

Problem-solver

Collaborative

Education

Bachelor's degree Life Sciences or equivalent

RN qualification

Tools

CTMS

eTMF

Job description

ICON is seeking a Clinical Research Associate to join the Cross Therapeutic team for the Northwest Region in the United States. You will be the primary liaison between investigational sites and sponsors, perform site visits, ensure ICH-GCP compliance, and maintain CTMS and eTMF documentation to support data quality and patient safety.

The ideal candidate has a Life Sciences degree or an RN, 2+ years of on-site monitoring in pharma/CRO, and travel up to 50%.