Clinical Trial Manager
Clinical Trial Manager (life sciences, 6 maanden, fulltime) in Utrecht via SIRE Life Sciences.
Bekijk bij SIRE Life Sciences B.V. (opent in een nieuw tabblad)
Eisen
- At least 5+ years of experience in Clinical Operations
- Strong experience working with CROs and coordinating trial activities
- Bachelor’s degree in a relevant field
- Solid understanding of regulated clinical trial delivery and quality expectations (e.g., ICH-GCP and internal SOPs)
- Comfortable working with trial documentation and budget monitoring
- Proven experience leading and managing clinical trials
Wensen
- Master’s degree
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Volledige omschrijving
Company: Our client is a leading organisation in the life sciences sector, focused on developing innovative therapies and running high-quality clinical research. The team works in a highly regulated environment and partners closely with internal stakeholders and external vendors to deliver trials efficiently, safely, and in full compliance.
Job Description: We are looking for a Clinical Trial Manager to take ownership of the operational delivery of clinical trials. This person will lead a cross-functional trial team, manage external partners such as CROs, and ensure trials are delivered on time, within budget, and to the required quality and compliance standards.
Responsibilities: Lead the trial-specific cross-functional Clinical Management Team, including oversight of CRO partners. Drive trial delivery to meet agreed timelines, budget, and quality expectations. Build strong collaboration with internal and external stakeholders to support smooth trial progress. Support selection of CROs and contribute to defining scope of work and expectations. Actively manage CRO performance throughout the trial and ensure clear communication and follow-up.
Ensure issues and risks are identified early and escalated appropriately to protect progress and quality. Support audits and inspections and help drive timely responses when needed. Maintain and manage trial budgets, including forecasting, accruals, and invoice coordination. Lead risk management activities related to patient safety and data integrity.
Requirements: Bachelor’s degree in a relevant field (Master’s degree preferred). At least 5+ years of experience in Clinical Operations. Proven experience leading and managing clinical trials. Strong experience working with CROs and coordinating trial activities. Solid understanding of regulated clinical trial delivery and quality expectations (e.g., ICH-GCP and internal SOPs). Comfortable working with trial documentation and budget monitoring.
Other Information: This is a great opportunity for an experienced clinical operations professional who enjoys owning trial delivery and working closely with a wide range of stakeholders. If you are interested and want to apply, please submit your application via the apply button below and contact me.
Contract: Temporary Full-Time Contract (6 Months).
Location: Utrecht, Utrecht.
Sector: Pharmaceuticals.
Start Date: 10/14/2026.
Job ref: 59241.
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