Senior RA Associate Consultant (Medical Devices) - EU MDR

ClinChoice(5 days ago)

RemoteContractSenior$35,000 - $43,000

About this role

ClinChoice is seeking a Senior Regulatory Affairs Associate Consultant specializing in medical devices with a focus on EU MDR. The role involves collaboration with project teams, document management, and regulatory compliance within a global CRO environment. It offers a remote option in Toronto, Ontario, on a 12-month contract basis.

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Required Skills

Regulatory Affairs
EU MDR
Medical Devices
Quality Control
Document Management
PLM
Adobe PDF
ISO13485
FDA Regulations
Microsoft Office

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.

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