Clinical Research Associate II – Remote (Chile)

About the role

Syneos Health is seeking a CRA II to support multi‑sponsor clinical studies on a remote basis for sites in Chile. The role involves site qualification, monitoring, data verification and ensuring compliance with regulatory and protocol requirements.

Key responsibilities

• Perform site qualification, initiation, interim monitoring, and close‑out visits remotely, ensuring adherence to ICH‑GCP and protocol.
• Review source documents, verify data entered in case report forms, and resolve queries within agreed timelines.
• Manage investigational product inventory, reconciliation, and compliance with storage and dispensing requirements.
• Maintain Investigator Site Files, reconcile with Trial Master Files, and support audit readiness.
• Support subject recruitment, retention, and awareness strategies, and document activities per SOPs.

Required profile

• Bachelor’s degree or RN in a related field, or equivalent experience.
• Knowledge of Good Clinical Practice, ICH guidelines and local regulatory requirements.
• Strong computer proficiency and ability to adopt new technologies.
• Excellent communication and interpersonal skills.
• Willingness to travel up to 75% of the time if required.

Required skills

• ICH/GCP compliance
• Electronic Data Capture (EDC) systems
• Source document review
• Query resolution techniques
• Investigational product handling