Regulatory Manager, Clinical Trials Regulatory Management- Home-Based, Emea  

Prepares and/or reviews regulatory documents to support clinical trial submissions.
Independently provides regulatory support for complex projects and programsRESPONSIBILITIES Acts as a Clinical Trial Regulatory Manager (CTRM) on complex clinical trial projects or programs and may act as a Regulatory Oversight for a key customerAbility to administratively and technically/scientifically review core scientific documentation and feedback gap analysis to customers.Ability to write scientific documents e.g. Investigational Medicinal Product Dossier, clinical trial justificationsMay strategically plan...