Clinical Research Associate - Denmark/Nordics Travel

Syneos Health Denmark ApS; Denmark; Remote; DKK 550,000 - 750,000; Full time

Job summary

Syneos Health Denmark ApS seeks an experienced Clinical Research Associate to work in Denmark. You will perform site qualification, initiation, monitoring, management and close-out visits, on-site or remote, ensuring GCP compliance and high-quality data.

You will support subject recruitment and site readiness, maintain ISF/TMF accuracy, and collaborate with sponsors and cross-functional teams across the Nordics.

Qualifications

• Bachelor’s degree or RN in related field.
• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Good computer skills; ability to embrace new technologies.
• Previous monitoring experience.
• Excellent communication, presentation and interpersonal skills.
• Fluency in Danish and English; understanding of Swedish/Norwegian is a plus.
• Ability to travel up to 75% regularly.
• Cross-border monitoring in the Nordics is possible.

Responsibilities

• Perform site qualification, initiation, interim monitoring, site management and close-out visits (on-site or remote).
• Assess site performance, communicate issues to the project team and develop action plans.
• Maintain knowledge of ICH-GCP guidelines, regulations and SOPs; ensure informed consent processes.
• Verify clinical data entry, perform source data verification and drive query resolution.
• Support site training, ISF/TMF reconciliation, patient recruitment and retention strategies.
• Prepare for Investigator Meetings and sponsor meetings; participate in training and audit readiness.

Skills

Communication skills

GCP knowledge

Computer skills

Monitoring experience

Fluent Danish

Fluent English

Travel up to 75%

Nordic cross-border monitoring

Education

Bachelor’s degree or RN in a related field

Job description

Syneos Health Denmark ApS seeks an experienced Clinical Research Associate to work in Denmark. You will perform site qualification, initiation, monitoring, management and close-out visits, on-site or remote, ensuring GCP compliance and high-quality data.

You will support subject recruitment and site readiness, maintain ISF/TMF accuracy, and collaborate with sponsors and cross-functional teams across the Nordics.