Senior RA Associate Consultant - EU MDR (Medical Devices)

ClinChoice(7 days ago)

RemoteContractSenior$51,800 - $63,640Regulatory Affairs

About this role

Senior Regulatory Affairs Associate Consultant supporting a major medical device client through a 12-month contract. The role focuses on EU MDR compliance and regulatory documentation management while working for a global CRO with the option to work remotely from Toronto, Ontario. The position involves representation of Regulatory Affairs on project teams and collaboration with cross-functional stakeholders.

View Original Listing

Required Skills

EU MDR
ISO13485
FDA Regulations
Microsoft Office
Document Management
Quality Control
Regulatory Submissions
Cross-Functional Collaboration
PLM
Adobe Acrobat

Qualifications

Bachelor's Degree (Life Sciences Preferred)

About ClinChoice

clinchoice.com

ClinChoice is a full‑service global contract research organization (CRO) that helps accelerate drug and medical device approvals to market. They offer end‑to‑end clinical development, regulatory strategy, and operational support across study design, execution, data management and safety to guide sponsors through all phases of development. With global site networks, therapeutic expertise and data‑driven processes, ClinChoice aims to shorten timelines and reduce risk for development programs. They partner with biotech, pharma and device companies to navigate complex regulatory pathways and bring safer products to patients.