ClinChoice Canada Inc. is seeking a Sr. Regulatory Affairs Associate – CONSULTANT to join its global CRO team on a 12‑month contract.
You will work closely with regulatory project teams to review, draft, and manage Technical Documents for EU MDR and other regulatory needs, ensuring accuracy and timely delivery. The role requires at least 2 years in Regulatory Affairs focused on EU MDR, knowledge of ISO13485 and FDA regulations, and strong English communication.
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Senior Regulatory Affairs Consultant – EU MDR Expert employer: ClinChoice
ClinChoice Canada Inc. is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals in the clinical data management field. With a strong emphasis on employee growth and development, team members are encouraged to enhance their skills through ongoing training and mentorship opportunities. Located in Ontario, the company offers a hybrid work model that promotes work-life balance while contributing to impactful clinical trials.
