Join the team that’s transforming clinical research. Advarra is hiring a detail-driven Coordinator to support IRB meetings, consent form compliance, and regulatory precision—all from the comfort of home.
✅ Position Highlights:
• Full-time | 100% Remote (U.S. or Canada)
• Salary Range: $36,200–$61,500 USD
• Eligible for variable bonus, health benefits, PTO, and paid holidays
🔎 What You’ll Own:
• Review and assign IRB submissions for full board review
• Prep IRB meeting materials, consent forms, and determination memos
• Conduct quality control checks on consent forms and documentation
• Ensure compliance with U.S. and Canadian research regulations
• Attend a minimum of four IRB meetings/month to deepen your expertise
• Collaborate across teams to implement feedback and edits
• Continuously enhance regulatory knowledge and propose process improvements
🎯 Must-Have Traits & Experience:
• Bachelor’s degree + 1 year of IRB or clinical research experience
OR
• Associate’s degree + 4 years of IRB or clinical research experience
• Proficiency in MS Word and Outlook
• Basic knowledge of FDA, HHS, TCPS2, ICH GCP, and human research protection
• Strong written and verbal communication skills
✨ Nice-to-Haves:
• Experience with Excel, Slack, Zoom, RingCentral, and proprietary platforms
• Ability to convert technical/medical jargon into clear lay terms
• Organized, detail-obsessed, and deadline-focused
• Comfort with editing, proofreading, and collaborating across departments
• Public speaking confidence and cross-functional team skills
🌍 Why It’s a Win for Remote Professionals:
• Work at the forefront of ethical clinical research
• Be part of a mission-driven company committed to health innovation
• Join a culture that values empathy, collaboration, and diverse perspectives
• Enjoy flexibility and autonomy while contributing to meaningful impact
✍️ Call to Action:
Ready to elevate ethical clinical research while working remotely? Apply now and help power a connected ecosystem that’s improving lives across the globe.