Clinical Trial Manager – Future Roles

About the role

Syneos Health is seeking a Clinical Trial Manager to support future clinical studies in Australia. The role involves overseeing site qualification, initiation, monitoring, and close‑out activities, ensuring compliance with regulatory and protocol requirements.

Key responsibilities

• Perform site qualification, initiation, interim monitoring, and close‑out visits, both on‑site and remotely.
• Assess site performance, manage queries, and ensure accurate data entry into case report forms.
• Oversee investigational product inventory, reconciliation, and compliance with storage and dispensing protocols.
• Maintain Investigator Site Files, reconcile with Trial Master Files, and support audit readiness.
• Coordinate recruitment, retention, and site training; act as liaison between study sites and central monitoring teams.

Required profile

• Bachelor’s degree or RN in a related field, or equivalent experience.
• Strong knowledge of Good Clinical Practice (GCP) and ICH guidelines.
• Excellent communication and interpersonal skills.
• Willingness to travel up to 75% of the time.

Required skills

• Good Clinical Practice (GCP) / ICH guideline expertise.
• Electronic data capture (EDC) systems proficiency.
• Source document review and data verification.
• Investigational product handling and inventory management.