Position Summary The EU CTR Submission Specialist is responsible for planning, preparing, managing, and maintaining regulatory submissions for clinical trials in compliance with EU Clinical Trial Regulation (EU CTR 536/2014) via the Clinical Trials Information System (CTIS). This role covers the ent......
Hiring In Warsaw, Poland
full-time Sourced
General 3-yearsBiogen In...ScraperLoicx
Job Description Summary The Senior Associate, Submission Specialist plays an essential role within the content team and is accountable for End-to-End submission support of promotional assets for the US Marketing and operations team in Medical Legal Regulatory tool (FUSE) Job Description Key Respon......