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Clinical Scientist
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Full-time
- The ideal candidate should have relevant experience in GCP/ICH, clinical operations, and enjoy fast-paced, collaborative and vibrant startup culture.
- Collaborate and liaise with clinical sites to support overall clinical trial participant management, data review activities and facilitating issue resolution
- Support the development of data review plans and monitor clinical data for specific trends.
- Perform ongoing and timely clinical trial data review in the form of listings, tables, patient profiles and live clinical database
- Develop site and CRA protocol- and product-related training materials and present these at SIV and Investigator meetings
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