Clinical Research Associate I (Fully Remote)

AbbVie; United States; Remote; USD 70,000 - 100,000; Full time

Job summary

AbbVie is seeking a Clinical Research Monitor to ensure GCP and SOP compliance across trials. You will conduct site qualification, initiation, interim, and closeout visits, train site staff, and proactively manage performance.

The role requires a health-related degree and knowledge of ICH/GCP, with strong planning, analytical, and communication skills. This position is remote based in Madrid with travel to study sites, operating in a dynamic, deadline-driven environment.

Qualifications

• Health-related degree required.
• Knowledge of ICH/GCP guidelines and applicable regulations.
• Strong planning, analytical, and communication skills.
• Remote based in Madrid with travel to study sites.
• Dynamic environment with competing projects and deadlines.

Responsibilities

• Monitor clinical trials and ensure compliance with regulations, GCP, and SOPs.
• Conduct site qualification, initiation, interim, and closeout visits.
• Train site staff and proactively manage site performance.

Skills

Clinical research monitoring

ICH/GCP knowledge

Planning

Analysis

Communication

Education

Health-related degree

Job description

• Monitor clinical trials and ensure compliance with regulations, GCP, and SOPs.
• Conduct site qualification, initiation, interim, and closeout visits.
• Train site staff and proactively manage site performance.

Qualifications:

• Health-related degree with clinical research monitoring experience.
• Knowledge of ICH/GCP guidelines and applicable regulations.
• Strong planning, analytical, and communication skills.
• Remote based in Madrid with travel to study sites.
• Dynamic environment with competing projects and deadlines.

AbbVie

AbbVie discovers and delivers innovative medicines and solutions across immunology, oncology, and neuroscience. It is a global biopharmaceutical company committed to integrity, innovation, and transforming lives.