CRA II, ICON Biotech, Home based, Netherlands ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
At ICON plc, we are a global healthcare intelligence and clinical research organization committed to driving innovation, excellence, and inclusion. Our mission is to advance clinical development and help bring life-changing, innovative treatments to patients worldwide.
We are currently seeking experienced ClinicalResearch Associate II (CRA II) professionals to join our dynamic and collaborative Biotech team.
Our Biotech division of over 8,000 professionals operates with the agility and mindset of a small to mid-sized biopharma company. We understand the unique pressures biotech organizations face in delivering innovative therapies to market. Through tailored teams and dedicated management, we partner closely with our biotech clients — engaging, collaborating, and sharing accountability to ensure successful clinical trial delivery.
This is a fully remote role based in The Netherlands, with national travel as required.
What You’ll Do:
Managing clinical studies in the Netherlands for Small and Medium sized Biotech sponsors, across multiple therapeutic areas.
Independently monitor Phase I–III clinical trials to ensure compliance with ICH-GCP and regulatory requirements
Conduct site qualification, initiation, monitoring, and close-out visits
Manage study documentation, regulatory submissions, and ethics/IRB approvals
Collaborate with cross-functional teams and site staff to ensure high-quality data and patient safety
Ensure study cost efficiency and timely issue resolution
What You Bring:
Life science degree or equivalent
2 years or more experience as a Clinical Research Associate, with an understanding of clinical trial processes and regulatory requirements within a CRO or Pharma environment.
Knowledge of clinical trial processes and regulatory standards
Excellent communication, organization, and problem-solving skills
Proficiency with clinical trial systems and tools
Fluency in Dutch and English both Spoken and Written.
This is a remote role with willingness to travel across Netherlands
Should possess a valid driver’s license.
ICON offers comprehensive CRA development programs that provide structured learning pathways appropriate for each role within the CRA function where you can continue your professional development.
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
ICON plc is a world-leading healthcare intelligence and clinical research organization that specializes in designing and analyzing clinical trials, managing complex medical data, and advancing innovative treatments and therapies. The company serves the pharmaceutical and healthcare industries by providing comprehensive clinical research services, including site qualification, monitoring, and protocol compliance across global clinical development programs. ICON offers expertise in clinical data management, data standards (CDISC, CDASH, SDTM, ADaM), and regulatory submissions for sponsors conducting clinical trials. The organization is committed to fostering an inclusive environment that drives innovation and excellence in clinical development while supporting the advancement of new therapeutic solutions.
