CRA - Future Roles (Denmark)

Overview

Clinical Research Associate role supporting clinical and real-world late-phase studies in Denmark, from site identification through close-out. The position may involve on-site and remote monitoring and up to 75% travel.

What you'll do

• Perform site qualification, initiation, monitoring, management and close-out visits.
• Assess site performance, compliance, risks and required corrective actions.
• Review source documents, medical records, case report forms and electronic data.
• Manage queries and track observations, action items and site status to resolution.
• Review investigational product handling and Investigator Site File completeness.
• Support recruitment, retention, investigator meetings, training and audit readiness.
• Collaborate with sites, sponsors, affiliates and project teams throughout the study lifecycle.

What you'll need

• Bachelor’s degree or RN in a related field, or equivalent education, training and experience.
• Knowledge of Good Clinical Practice, ICH Guidelines and applicable regulations.
• Good computer skills and ability to use new technologies.
• Strong communication, presentation and interpersonal skills.
• Ability to manage regular travel of up to 75%.

Nice to have

• Knowledge of local requirements for real-world late-phase study designs.
• Ability to train junior staff.
• Local knowledge of treatment patterns, patient advocacy and healthcare provider associations.

Details

• Location: Denmark.
• Monitoring may be performed on-site or remotely.
• This posting is for a possible future opportunity and is intended to build a talent pipeline.