IQVIA LLC seeks a skilled clinical monitoring professional to conduct on-site visits across sites, ensuring protocol adherence and regulatory compliance. You will manage site communications, training, and quality issues, contributing to project success.
The role requires travel, strong knowledge of GCP/ICH, and experience coordinating regulatory submissions and data handling across multiple studies. Join IQVIA to support innovative medical treatments and patient outcomes.
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Slough, Berkshire
IQVIA UK's Site Management (multi-sponsor) team is growing and seeking junior and experienced Clinical Research Associates.
Manchester, Lancashire
IQVIA UK's Site Management (multi-sponsor) team is growing and seeking junior and experienced Clinical Research Associates.
Lancashire
IQVIA UK's Site Management (multi-sponsor) team is growing and seeking junior and experienced Clinical Research Associates.
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