Location: Montreal
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.
We are looking to fill the Global Regulatory Affairs Specialist
- Flexible Hours position at Indero in Montreal, QC, Canada.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the Global Regulatory Affairs Specialist
- Flexible Hours role at Indero, based in Montreal, QC, Canada.
The Global Regulatory Affairs Specialist
- Flexible Hours role at Indero is now open for applications in Montreal, QC, Canada.
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