Clinical Research Associate 2 , Multi-Sponsor - Based in Portugal

IQVIA · Lisbon, Portugal

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Clinical OperationsFull-timeCompany career page

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Role summary

Clinical Research Associate position in Lisbon supporting multi-sponsor clinical trials. Responsibilities include site selection, monitoring, recruitment planning, and regulatory compliance oversight across study sites.

What they're looking for

University degree in scientific or healthcare discipline
Minimum 2 years on-site clinical monitoring experience
Proficiency in MS Office and standard computer applications
Fluent in Portuguese and English
Strong organizational and problem-solving capabilities
Valid class B driver's license
Willingness to travel regularly

What you'll be doing

Conduct site selection, initiation, monitoring, and closeout visits
Develop and support subject recruitment planning activities
Assess site compliance with GCP and ICH regulatory guidelines
Track regulatory submissions, enrollment metrics, case report forms, and data queries
Collaborate with site staff and client representatives on study operations

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Date posted16 days ago

Last source check1 day ago

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