About the job
We’re partnering with a global leader in medical technologies to hire a Clinical Affairs Specialist who will play a critical role in supporting clinical investigations and post-market surveillance activities across a portfolio of innovative cardiovascular devices.
Why this opportunity stands out:
- Remote role with a flexible, build-your-own schedule
- High-impact work supporting life-saving technologies
- Competitive compensation and comprehensive benefits package
- Opportunity to travel extensively (75%)—primarily across the West Coast
Key Responsibilities:
- Support clinical trial operations including site initiation, monitoring, and closeout activities
- Conduct post-market clinical follow-up (PMCF) visits and support data collection
- Provide hands-on product support in the field, including device troubleshooting and user guidance
- Serve as a liaison between clinical sites, CROs, and internal teams
- Ensure compliance with GCP, regulatory requirements, and company SOPs
- Prepare and maintain clinical documentation for regulatory submissions
Qualifications:
- Active RN license (required)
- Bachelor’s degree in nursing, life sciences, or a health-related field
- 4+ years of nursing experience
- Direct experience working with balloon pumps—including setup, operation, and takedown—is required
- Willingness and ability to travel 75% of the time, focused on the West Coast
Location:
- Remote – U.S. based. Candidates residing in California, Oregon, or Washington will be given priority consideration due to the travel region.