Senior CRA: Site Engagement and Risk-Based Monitoring

Regulatory Jobs; Seattle (WA); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical/dental/vision insurance

401(k) plan

Job summary

AbbVie is seeking a Clinical Research Associate to engage investigative sites, ensure protocol adherence, and support patient safety. The role emphasizes collaboration with investigators and staff to maintain data integrity and trial quality.

The candidate should have a health-related degree and at least 1 year of clinical research monitoring experience, with strong knowledge of ICH/GCP and site engagement strategies.

Qualifications

• Minimum of 1 year of clinically related experience, including at least 6 months in clinical research monitoring.
• Advanced knowledge of ICH/GCP Guidelines and applicable policies.
• Strong collaboration with internal and external stakeholders across functions.

Responsibilities

• Serve as primary contact for investigative sites and ensure trial readiness and safety.
• Train and motivate site staff and principal investigators on trial goals and patient care principles.
• Monitor site performance in line with protocol, GCP, and regulatory requirements.

Skills

Cross-functional collaboration

Regulatory knowledge

Problem solving

Education

Health-related tertiary qualification

Job description

AbbVie is seeking a Clinical Research Associate to engage investigative sites, ensure protocol adherence, and support patient safety. The role emphasizes collaboration with investigators and staff to maintain data integrity and trial quality.

The candidate should have a health-related degree and at least 1 year of clinical research monitoring experience, with strong knowledge of ICH/GCP and site engagement strategies.