Senior Clinical Research Associate

Senior CRA - Netherlands

Remote | Sponsor-Dedicated FSP Model | Bonus Scheme | Career Progression

Join a global CRO while becoming fully embedded within a leading sponsor environment.

This is an excellent opportunity for an experienced Senior CRA seeking greater study ownership, sponsor visibility and long-term career progression within a supportive and collaborative environment.

What Makes This Different?

Many sponsor-dedicated opportunities can become restrictive over time. This role is designed differently.

You'll gain all the benefits of working within a dedicated sponsor environment, including deeper study involvement, stronger stakeholder relationships and greater visibility, while retaining the support, development opportunities and career flexibility of a global CRO.

After 12 months, you'll have the opportunity to either remain within your current sponsor assignment or broaden your experience by moving to another sponsor programme.

You'll also benefit from a structured mentorship programme, embedded CRO leadership support and multiple defined promotion levels that make progression more achievable and transparent.

Why Join?

• Dedicated sponsor assignment
• Opportunity to rotate sponsors after 12 months
• Annual bonus scheme
• Company car or car allowance
• Embedded CRO manager support
• Structured mentoring programme
• Clearly defined career progression framework
• Collaborative local team environment
• Comprehensive benefits package
• Home office support

Key Responsibilities

• Conduct qualification, site selection, initiation, routine monitoring and close-out visits across assigned studies.
• Perform comprehensive source data verification (SDV) and source data review (SDR) activities to ensure data quality and patient safety.
• Evaluate site performance, protocol compliance and overall study conduct.
• Identify, investigate and escalate quality issues, protocol deviations and site risks appropriately.
• Review informed consent processes and ensure patient protection procedures are maintained.
• Verify investigational product accountability, storage requirements and site documentation.
• Ensure investigator site files remain inspection-ready throughout the study lifecycle.
• Support sites with recruitment, retention and study execution strategies.
• Review electronic CRFs and collaborate with sites to resolve data queries efficiently.
• Produce high-quality monitoring reports and follow-up correspondence within required timelines.
• Build effective working relationships with investigators, study coordinators and key opinion leaders.
• Participate in investigator meetings, project meetings and sponsor governance discussions.
• Support audit and inspection readiness activities.
• Share best practice across study teams and provide mentorship and guidance to junior CRAs where appropriate.

Experience & Requirements

• Significant independent monitoring experience.
• Strong knowledge of ICH-GCP and European clinical trial regulations.
• Experience managing investigator sites independently.
• Excellent issue management and stakeholder engagement capabilities.
• Fluent Dutch and English.
• Oncology experience preferred but not essential.
• Ability to travel throughout the Netherlands.