Clinical Research Associate II / Senior CRA (Spanish, Portuguese & English fluency)
Core
Conducts on-site and remote monitoring visits (Pre-Study, Initiation, Interim, Close-Out) in Spain and Portugal to ensure investigational sites are adequate for clinical study conduct.
Role type
Senior Clinical Research Associate (CRA)
Builds
Clinical trial data and site compliance for rare disease and oncology studies
Domain
Clinical Research / Life Sciences / Oncology / Rare Disease
Required skills
On-site monitoring, Phase 2/3 trial experience, complex trial management (oncology/rare disease), regulatory submission support, site staff training, travel
Preferred skills
Experience with complex trials, dynamic team environment adaptability
Technologies
Clinical trial management systems, regulatory submission platforms
Responsibilities
Perform Pre-Study, Initiation, Interim, and Close-Out monitoring visits; Verify investigator qualifications and site resources; Train investigational site staff; Support preparation of regulatory and EC submissions
