Site Specialist II
145 ICR Spain - SPA · Madrid, Spain
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.
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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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