Clinicical Research Associate Utrecht • Talentmark

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Clinical Research Associate – Utrecht – 50/50 homebased

Are you looking for a CRA role where you can make a real impact and be involved in every step of the clinical trial process?
Our client is a dynamic Clinical Research Organization (CRO) providing high-quality services to the pharmaceutical, biotech, and medical device industries. To support our expanding portfolio, we’re looking for a motivated Clinical Research Associate (CRA) to join the team in the Netherlands.

Within this company, you won’t be limited to routine monitoring. Instead, you’ll be a core member of their clinical operations team, working across all stages of the clinical trial lifecycle. From feasibility to final close-out, you’ll play a hands-on role in shaping trial success. This is an exciting opportunity for someone who thrives in a dynamic environment and values autonomy, variety, and real impact.

Key Responsibilities

• Conduct and manage all types of site visits (pre-study, initiation, monitoring, and close-out)
• Participate in site feasibility, selection, and start-up activities
• Support ethics and regulatory submissions
• Review and manage essential clinical documents (e.g., ICFs, protocols, CRFs)
• Ensure compliance with ICH-GCP, local regulations, and study protocols
• Build strong site relationships and act as the main point of contact for investigators
• Identify and resolve site-level issues proactively
• Maintain accurate and up-to-date study tracking systems and reports
• Collaborate closely with project managers, lead CRAs, and other functional teams
• Contribute to continuous process improvement within clinical operations

Why join?

Unlike large CROs, they are a close-knit team of 15 professionals. This means:

• You’ll work side-by-side with project managers and lead CRAs
• You’ll be involved from start to finish—from feasibility and site selection, to submissions, document development, and all types of site visits
• You’ll gain broad experience—not just monitoring
• You’ll have room to grow: your responsibilities will evolve as you do
• With approximately 4–6 monitoring visits per month, your role is diverse, engaging, and deeply hands-on.

What You Bring

• A relevant degree (BSc or MSc in biomedical sciences or similar)
• At least 1 year of clinical experience in the pharmaceutical or biotech industry
• Understanding of ICH-GCP and applicable regulatory guidelines
• A proactive, flexible, and entrepreneurial mindset
• Fluency in Dutch and English (both written and spoken)

What You’ll Get

• A role that grows with you
• An open, collaborative work culture
• The opportunity to shape trial success, not just observe it
• Direct involvement with innovative, early-phase clinical research

Interested? Please respond via this page!

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