Senior Site Specialist

What You Will Do:

• Managing advanced site-level activities for investigator sites across the Benelux region, including essential document collection, review, and maintenance for assigned sites and studies.
• Supporting local study start-up activities, including CTIS submissions, regulatory document collection, and coordination of country-specific requirements.
• Acting as a primary liaison for site staff on operational questions, documentation requirements, regulatory processes, and study procedures.
• Ensuring accurate and timely updates of site status, regulatory information, and study data within clinical trial management systems and trackers.
• Coordinating site visits, meetings, and communications with investigator sites in collaboration with CRAs, start-up teams, and project stakeholders.
• Identifying opportunities to improve site workflows, enhance site engagement, and contribute to process improvement initiatives.
• Providing guidance and mentorship to junior team members on site support processes, regulatory requirements, and best practices.

Your Profile:

• Bachelor's degree in Life Sciences, Healthcare, Business, or a related field, or equivalent experience in clinical research.
• Strong experience in site support, clinical trial administration, study start-up, or similar roles within a CRO, pharmaceutical company, or healthcare environment.
• Working knowledge of clinical trial processes, ICH-GCP guidelines, and site documentation requirements.
• Experience supporting regulatory activities, including CTIS submissions and country-specific start-up requirements, is highly desirable.
• Excellent organizational skills and attention to detail, with the ability to manage multiple sites, studies, and competing priorities.
• Strong communication and interpersonal skills, with a customer-focused approach to investigator site support.
• Ability to work independently and collaboratively, with experience supporting or mentoring junior colleagues.
• Fluency in English
• Fluency in Dutch or French is an advantage, as the role involves regular communication and partnership with investigator sites, site personnel, regulatory bodies, and stakeholders across the Benelux region.

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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