Senior Clinical Research Associate 1 - Based In Portugal
IQVIA UK
Portugal
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Site selection initiation monitoring close-out visits
Good clinical practice international conference on harmonization guidelines
Tracking regulatory submissions case report form completion
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IQVIA UK is seeking a Senior Clinical Research Associate in Portugal, responsible for site monitoring, regulatory compliance, and collaboration with study sites. The ideal candidate should have a scientific degree, at least three years of on-site monitoring experience, and excellent communication skills in both Portuguese and English.
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Job Summary
The role involves performing site selection, initiation, monitoring, and close-out visits while supporting subject recruitment plans.
Candidates must evaluate site practices against Good Clinical Practice and International Conference on Harmonization guidelines.
The company offers a company car, mobile phone, flexible work schedules, and resources for career growth.
Matching Summary
Match Score: 75
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IQVIA UK is seeking a Senior Clinical Research Associate in Portugal, responsible for site monitoring, regulatory compliance, and collaboration with study sites. The ideal candidate should have a scientific degree, at least three years of on-site monitoring experience, and excellent communication skills in both Portuguese and English.
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Skills & Requirements
Must-have
Site selection initiation monitoring close-out visits
Good Clinical Practice International Conference on Harmonization guidelines
Tracking regulatory submissions case report form completion
Excellent command of Portuguese and English language
Nice-to-have
Organizational time management and problem-solving skills
Establish effective working relationships with coworkers
Flexibility to travel within Portugal region
Key Requirements
University degree in scientific discipline or health care