Clinical Trial Manager

Opdracht voor een Clinical Trial Manager.

Opdrachtgever: verborgen voor premium leden.

Standplaats: Utrecht, regio Utrecht/Flevoland.

Duur opdracht: 6 maanden.

Indicatie uurtarief: niet vermeld.

Aantal uren per week: niet vermeld.

Opleidingsniveau: Bachelor / HBO.

Sector: Farmaceutische & Chemisch.

Laatste update: 15 oktober 2026. Profiel van de geschikte interim professional: Bachelor's degree in a related discipline, with a Master's degree regarded as an advantage; Minimum of 5 years' experience within Clinical Operations; Track record of leading and managing clinical trials; Background in collaborating with CROs and coordinating trial-related activities; Solid understanding of regulated clinical trial delivery, including ICH-GCP and internal SOPs; Comfortable handling trial documentation and budget monitoring.

Taken & verantwoordelijkheden: Lead the cross-functional clinical trial team, including oversight of CRO partners; Drive trial delivery against agreed timelines, budget and quality targets; Build collaboration with internal and external stakeholders to support trial progress; Support CRO selection and help define scope of work and expectations; Manage CRO performance and maintain clear communication and follow-up; Identify and escalate risks and issues to safeguard progress and quality; Support audits and inspections and help ensure timely responses; Maintain trial budgets, including forecasting, accruals and invoice coordination; Direct risk management efforts concerning patient safety and data integrity.