Freelance CRA - Spain

IQVIA · Barcelona, Spain +1 more

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Clinical OperationsPart-timeCompany career page

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Role summary

IQVIA seeks two experienced Clinical Research Associates for freelance positions supporting Phase III studies across Spain. Each role involves approximately 18 hours per week of site monitoring activities for approximately six months, starting as soon as possible.

What they're looking for

Minimum 2 years of CRA monitoring experience
Previous Phase III clinical trial experience
Strong knowledge of ICH-GCP and clinical trial processes
Fluent in Spanish and English
Ability to work independently with excellent communication skills
Willingness to travel within Spain 2-3 times monthly

What you'll be doing

Conduct interim monitoring visits at approximately 10 clinical trial sites
Ensure protocol adherence and ICH-GCP compliance across assigned sites
Verify source documents and review study data for accuracy
Identify site issues and collaborate on action plans for resolution
Support site investigators and personnel with study implementation

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Date posted4 days ago

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