CRA II / Senior CRA - Early Phase

This is a hybrid or Remote role based in the Netherlands. Candidates should be located within a reasonable commuting distance of Groningen and able to attend ICON's Early Phase Clinical Research Centre as required.

What You Will Do

Your focus will be on delivering high-quality monitoring activities, ensuring site performance and maintaining inspection readiness across your studies.

• Independently manage assigned investigative sites, ensuring protocol compliance, data quality and patient safety.
• Conduct onsite and remote monitoring visits in accordance with study requirements and risk-based monitoring strategies.
• Verify informed consent processes, source documentation and adherence to study protocols.
• Maintain site essential documentation, including ISF and TMF records, ensuring continuous inspection readiness.
• Identify, escalate and support resolution of study risks, issues and data discrepancies.
• Build strong relationships with investigators, site staff and sponsor representatives to drive study success.
• Support site staff through training, guidance and ongoing communication throughout the study lifecycle.
• Contribute to regulatory submissions, audit preparation and inspection readiness activities where required.
• Collaborate closely with Clinical Operations, Project Management and cross-functional study teams to achieve study milestones and recruitment goals.
• Ensure studies are conducted in accordance with ICH-GCP, protocol requirements, ICON and sponsor SOPs, and applicable regulatory requirements.

Your Profile

You will have strong clinical monitoring experience and the ability to work independently while managing competing priorities across multiple sites.

• Bachelor's degree in a scientific, healthcare or related discipline.
• Previous monitoring experience within a CRO, pharmaceutical company or clinical research environment.
• Strong understanding of ICH-GCP, clinical research regulations and clinical trial processes.
• Demonstrated ability to independently manage investigative sites and monitoring activities.
• Excellent communication and relationship-building skills with sites, sponsors and internal stakeholders.
• Strong organisational and prioritisation skills, with a high level of attention to detail.
• Experience working with electronic systems and clinical trial technology platforms.
• Ability to identify risks, propose solutions and escalate issues appropriately.
• Fluent English communication skills, both written and verbal.
• Willingness to travel as required for onsite monitoring visits and study activities.

#LI-SC1
#LI-Hybrid

#LI-Remote

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply