Senior Scientist, Nonclinical DMPK
Monitor and report on the progress of delegated clinical trials, which includes budgets and timelines. Prepare, oversee, and review documents that are related to assigned clinical study.
December 2, 2021
INSIGHTS
Author and review clinical and regulatory documents such as Study Protocols, ICFs, CSRs, IBs, Paediatric Investigation Plans, Briefing Books, Requests of Product Specific Waivers, applications for Orphan Drug Designations, and responses to Health Authorities; the documents should be accurate, suited for the intended audience and easy to read.
July 24, 2021
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Contact information
- Martinsgasse 20, CH-4051 Basel, Switzerland
- (+41) 78 889 3675
- signe.reidla@execruits.com