Clinical Research Associate II - Site Engagement & Monitoring

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

Benefits offered by this job

Healthcare benefits

401(k) plan

Performance bonuses

Job summary

AbbVie is seeking a Clinical Research Associate to support site engagement and monitoring across trials. You will partner with investigators and site staff to ensure protocol adherence, patient safety, and data integrity while driving study execution in a dynamic environment.

Candidate should have at least 1 year of clinical research monitoring experience, knowledge of GCP/ICH, and strong cross-functional collaboration skills.

Qualifications

• Minimum of 1 year of clinically related experience, including 6 months in clinical research monitoring of investigational trials.
• Familiar with risk-based monitoring approach, on-site and off-site monitoring.
• Knowledge of local regulatory and ICH/GCP guidelines and applicable policies.
• Strong cross-functional collaboration and organizational skills.
• Ability to mentor less experienced CRAs and participate in internal initiatives.

Responsibilities

• Serve as primary contact for investigative sites, providing contextual information on trials.
• Align and motivate site staff and Principal Investigator on trial goals and patient treatment principles.
• Conduct site evaluations, trainings, routine monitoring, and site closures per protocol and plans.
• Utilize site engagement tools and CRM to report progress and measure impact of engagement activities.
• Assess and mitigate site risks, ensuring data integrity and patient safety during study conduct.
• Support investigator payments and contract obligations as applicable.

Skills

Clinical monitoring

GCP/ICH

Site management

Regulatory knowledge

Education

Bachelor's degree in health sciences

Tools

CRM software

Job description

AbbVie is seeking a Clinical Research Associate to support site engagement and monitoring across trials. You will partner with investigators and site staff to ensure protocol adherence, patient safety, and data integrity while driving study execution in a dynamic environment.

Candidate should have at least 1 year of clinical research monitoring experience, knowledge of GCP/ICH, and strong cross-functional collaboration skills.