Clinical Trial Operations Manager

Opdrachtgever: Word lid of log in

Standplaats: Utrecht

Regio Utrecht, Flevoland

Duur opdracht in maanden: niet vermeld

Indicatie uurtarief: niet vermeld

Aantal uren per week: niet vermeld

Opleidingsniveau: Bachelor / HBO

Laatste update: 15 oktober 2026

Sector: Farmaceutische & Chemisch...

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Profiel van de geschikte interim professional:

Bachelor's or Master's degree in a relevant field, Master's preferred
A minimum of 5 years of experience in clinical operations
Substantial experience leading and managing clinical trials in pharma, biotech or clinical research
Track record coordinating trial activities, documentation and CRO relationships
Experience with trial budget monitoring, forecasting, accruals and invoice management
Solid knowledge of clinical trial regulations, ICH-GCP guidelines and quality requirements
Experience with risk management, patient safety, data integrity and audit/inspection readiness
Solid skills in project management, organisation and problem-solving
Excellent communication and stakeholder-management abilities across cross-functional and external teams
Proactive, structured and quality-focused working style, able to juggle multiple priorities

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