Innovaderm in Montreal is seeking a Regulatory Affairs Specialist to oversee EC, RA submissions and ensure regulatory compliance across CROs and partners. You will lead start-up activities for clinical trials and coordinate timelines with internal and external stakeholders.
The ideal candidate has 2–3 years CRO/Pharma regulatory experience with Health Canada and FDA, hands-on CTA and EC package readiness, and fluent English; French is a plus.
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📌 Global Regulatory Affairs Specialist - Flexible Hours (Montreal)
🏢 Indero
📍 Montreal
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