If you’ve owned adverse event processing in a clinical trial…this will feel very familiar.

We’re partnering with a structural heart company in Minnesota on a Clinical Safety Specialist role supporting an investigational heart valve program.

This is a fully onsite, execution-heavy role—not strategy, not oversight. You’re in it day-to-day, making sure nothing slips through the cracks.

Your role with the company:

• Processing AEs and SAEs end-to-end
• Reviewing source docs and chasing down missing data
• Writing safety narratives and supporting regulatory reporting
• Keeping everything inspection-ready at all times
• Working closely with Clinical, Regulatory, and Data teams onsite

Desired Profile:

• 3–5 years in clinical research / safety / pharmacovigilance
• Strong understanding of ICH-GCP + safety reporting
• Someone who is detail-obsessed and deadline-driven
• Comfortable in a fast-paced, high-volume environment

This is one of those roles where execution matters more than anything. If you’re someone who takes pride in clean data, tight timelines, and doing things right the first time, you’ll do well here.

📍 Minnesota (fully onsite)

If this sounds like you, or someone you trust, message me. I’ll give you a clear picture of the team and expectations.