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Global Study Director - CAR - T
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Full-time
- ICON plc is a world-leading healthcare intelligence and clinical research organization.
- Provide input to data management documents (e.g. Case Report Form, Data Validation Specifications), and interface with data management representatives and sites to facilitate the delivery of study data.
- Ensure that all study documents within scope of the GSM’s responsibilities are complete and verified for quality in the Trial Master File (TMF).
- Adhere to SOPs, global process, applicable Quality & Compliance manual documents and international guidelines (e.g. ICH-GCP) to ensure study is inspection ready at all times.
- University degree (or equivalent educational/work experience), preferably in medical or biological sciences or discipline associated with clinical research.
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