Clinical Research Associate – Future Roles (Denmark)

About the role

Syneos Health is seeking Clinical Research Associates for future projects in Denmark. The role involves site qualification, monitoring, data verification and investigational product management, either on‑site or remotely.

Key responsibilities

• Perform site qualification, initiation, interim monitoring, and close‑out visits ensuring compliance with ICH‑GCP, GPP and protocol requirements.
• Review source documents, verify data entered in case report forms, and resolve queries within agreed timelines.
• Manage investigational product inventory, reconciliation, storage, and dispensing according to protocol.
• Maintain Investigator Site Files, reconcile with Trial Master Files, and document activities through letters, reports and logs.
• Support recruitment, retention and patient awareness strategies, and act as liaison with site personnel.

Required profile

• Bachelor’s degree or RN in a related field, or equivalent experience.
• Knowledge of Good Clinical Practice, ICH Guidelines and relevant regulatory requirements.
• Excellent communication and interpersonal skills.
• Willingness to travel up to 75% of the time.

Required skills

• Good Clinical Practice (GCP) compliance
• ICH/GCP guideline knowledge
• Electronic data capture (eCRF) systems
• Investigational product handling and reconciliation