Clinical Research Associate I
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About the role
Office-based Clinical Research Associate I role in Barcelona, Spain. Responsibilities include onsite monitoring, study startup, CRF review, source document verification, query resolution, site management, feasibility research and stakeholder communication. Requires a College/University degree in Life Sciences, either at least 1 year as a Study Coordinator or 6 months as a Clinical Research Associate, English and Spanish proficiency, fluent Catalan, MS Office proficiency and willingness to travel. Permanent, full-time contract.
Key requirements
- • College/University degree in Life Sciences.
- • At least 0.5 years of relevant experience
- • Required skills: Clinical trial onsite monitoring, Study startup, CRF review, Source document verification, Query resolution, Clinical site communication and management, Vendor and in-house support coordination, Feasibility research, MS Office applications, Planning and multitasking, Communication, Collaboration, Problem-solving, Ability to travel
- • Required languages: English, Spanish, Catalan
Opportunity details
- • Workplace: On Site
- • Employment: Permanent
- • Posted: Sep 28, 2026
- • Original advert language: English
Full vacancy
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Job title: Clinical Research Associate I
Location: Barcelona, CT, Spain
Employment type: Full-time