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Senior Clinical Research Associate
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Full-time
- Acting as the Senior Clinical Research Associate for designated clinical studies, while providing leadership in the execution and management of clinical studies, to deliver high quality data to support Philips businesses.
- Ensuring the clinical studies are monitored and conducted according to procedures, including up to date and complete trial master files, regular review of data, and assurance that monitoring reports and follow-up documentation are completed and updates uploaded in Clinical Trial Management System (CTMS).
- Supporting electronic data capture (EDC) user acceptance testing and training as applicable.
- Overseeing and supporting the creation of trial master files, regulatory binders, source documents, including shipping and associated documentation.
- You’ve acquired 5+ years of experience in executing clinical studies in a healthcare, Clinical Research Organization or medical device setting.
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