Clinical Research Associate - Denmark

About the role

Syneos Health is recruiting an experienced Clinical Research Associate (CRA) for its multi-sponsor business unit in Denmark. The role covers site qualification, initiation, interim monitoring, site management and close-out visits, performed on-site or remotely, and ensures regulatory, ICH-GCP and protocol compliance.

Key responsibilities

• Evaluate site and site staff performance, escalate serious issues and develop action plans
• Verify informed consent, protect subject confidentiality and assess factors affecting safety and data integrity
• Review source documents and CRFs, resolve queries and verify electronic data capture compliance
• Check investigational product inventory, dispensing and administration, and ensure proper labelling, import and return
• Review the Investigator Site File, reconcile it with the Trial Master File and document site activities
• Support recruitment and retention, enter tracking data and manage site-level communication
• Act as liaison with sites, prepare for and attend investigator meetings and sponsor meetings, and support audit readiness

Required profile

• Bachelor's degree or RN in a related field, or equivalent education, training and experience
• Previous monitoring experience
• Fluency in Danish and English; Swedish and Norwegian preferred
• Ability to travel regularly up to 75%, with possible cross-border monitoring in the Nordics

Required skills

• Good computer skills and willingness to adopt new technologies
• Knowledge of ICH-GCP and other regulatory requirements
• Excellent communication, presentation and interpersonal skills