ClinChoice is seeking a Sr. Regulatory Affairs Associate – CONSULTANT for a 12-month contract in Canada. The role collaborates with the regulatory team to manage TDs per EU MDR and other regulatory requirements, with duties spanning document creation, QA, and cross-functional coordination. The ideal candidate has a life sciences degree and 2+ years in EU MDR regulatory affairs, plus solid English communication and MS Office skills. Remote/contract arrangements are indicated. #J-18808-Ljbffr