Clinical Trial Manager – Neuroscience

About the role

The Clinical Trial Manager (CTM) will lead neuroscience studies of low to moderate complexity, ensuring clean, evaluable data are delivered on time and within budget. Reporting to the project manager, the CTM works closely with cross‑functional teams to meet client expectations and maintain regulatory compliance.

Key responsibilities

• Manage all clinical operational and quality aspects of assigned studies in compliance with ICH GCP.
• Develop and maintain clinical tools such as Monitoring Plans, Monitoring Guidelines, and Data Quality Plans.
• Prepare and organise sections of the Trial Master File (TMF) and ensure timely archiving of study documents.
• Collaborate with project managers to present at client meetings, bid defenses, and hand‑off sessions.
• Lead team meetings, monitor timelines, track metrics, and implement recovery actions when needed.
• Implement and train staff on standardized clinical monitoring processes.
• Conduct site visits, address protocol queries, and manage CRF collection and query resolution.
• Oversee project financials in smaller regions and ensure activities stay within contract scope.

Required profile

• Proven experience managing clinical trials, preferably in neuroscience.
• Strong knowledge of ICH GCP guidelines and clinical trial regulations.
• Ability to manage study budgets, timelines, and deliverables.
• Excellent communication skills for interaction with sites, sponsors, and internal teams.

Required skills

What we offer

• Opportunity to work on innovative neuroscience projects.
• Collaborative environment with experienced clinical professionals.
• Professional development and training in clinical monitoring standards.