Clinical Research Associate II

 Posted 21 days ago
     
2-5 years experience
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AI Summary

Independently monitor Phase II-IV clinical trials to ensure compliance with ICH-GCP and regulatory requirements. Manage site visits, study documentation, and collaborate with cross-functional teams to ensure patient safety and data quality.
CRA II / Senior CRA, ICON Large Pharma, 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 partner with the world’s leading pharmaceutical organizations to accelerate the development of transformative therapies. Within our Large Pharma division, we deliver global scale, operational excellence, and deep therapeutic expertise across complex clinical programs.

We are currently seeking a Clinical Research Associate II or Senior Clinical Research Associate to join our established Large Pharma team in the Netherlands. This is a fully remote position with travel across the Netherlands.

What You’ll Do:

  • Managing clinical studies for leading pharmaceuticals, across multiple therapeutic areas such as Oncology Neurology, Obesity and Rare Diseases.
  • Independently monitor Phase II–IV 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
  • Mentor and support site personnel and junior CRAs
  • Ensure study cost efficiency and timely issue resolution

What You Bring:

  • Life science degree or equivalent
  • 2+ years (CRA II) or 4+ years (Senior CRA) independent monitoring experience in Phase II–IV trials
  • Strong 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.

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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

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