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Site Specialist II

145 ICR Spain - SPA · Madrid, Spain

Entry LevelExternal listingfull-time15 days ago

About The Role

Site Specialist II - Nordic languages - home or office based

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.

We are currently seeking a Site Specialist II to join our diverse and dynamic Site Activation team at ICON . In this role, you will play a meaningful part in bringing clinical research to life by supporting investigator sites across the Nordic region (Sweden, Norway, Denmark, and Finland) .

As a Site Specialist II at ICON, you will be at the heart of study start-up, ensuring essential documentation and site activation activities are delivered efficiently, compliantly, and with a strong sense of partnership. Your work will directly contribute to accelerating the delivery of innovative medicines to patients worldwide.

What You Will Be Doing

  • Coordinating site-level document collection, review, and maintenance, ensuring accuracy and compliance for assigned sites or studies.
  • Acting as an operational liaison for site staff on documentation, systems, and process-related questions.
  • Maintaining up-to-date site status, metrics, and key milestones in clinical trial management tools.
  • Supporting planning and logistics for site meetings, investigator meetings, and monitoring visits.
  • Identifying opportunities to streamline site workflows and contributing to process improvement initiatives.

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  • Providing guidance to Site Specialist I or junior colleagues, sharing best practices and supporting their development.

Your Profile

  • Bachelor’s degree in life sciences, healthcare, business, or a related field, or equivalent experience.
  • Relevant experience in site support, clinical administration, or similar roles within CRO, pharma, or healthcare.
  • Good understanding of clinical trial processes, GCP, and site documentation requirements.
  • Fluency in English and at least one Nordic language ( Swedish, Norwegian, Danish, or Finnish ); additional Nordic languages are an advantage.
  • Strong organizational skills and attention to detail, with the ability to manage multiple priorities and timelines in a fast-paced environment.
  • Clear and confident communication skills, with a collaborative and site-centric mindset.

#LI-MK1
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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