Opportunity
Senior Clinical Research Associate
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About the role
Home-based Senior Clinical Research Associate role in the Netherlands, responsible for onsite monitoring visits, study startup, CRF and source document review, site management, quality control, feasibility work, and regulatory submission support. Requires a BSc or MSc in Life Sciences or similar, Dutch and English fluency, Dutch monitoring experience, Phase II/III monitoring experience, a full clean driver’s license, and travel ability.
Key requirements
- • BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience
- • Required skills: Independent on-site monitoring experience in the Netherlands, Experience in all types of monitoring visits in Phase II and/or III, Strong written and verbal communication skills, Advanced knowledge of MS Office, Communication, collaboration, and problem-solving skills, Ability to multitask and work in a dynamic team environment, Ability to travel
- • Required languages: Dutch, English
- • Professional registration/licence (Netherlands)
Opportunity details
- • Workplace: Remote
- • Posted: Sep 30, 2026
- • Original advert language: English
Full vacancy
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See original vacancy ↗Employer’s role description
Job title: Senior Clinical Research Associate
Location: Utrecht, UT, Netherlands