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Clinical Research Associate II

836 PRA Group BV · Remote, ZEN, Netherlands

Clinical TrialsJunior LevelRemoteExternal listingfull-time9 days ago

About The Role

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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