Clinical Trial Coordinator

What you'd do

• Call inbound leads for our clinical trials and screen them against study criteria
• Run the informed consent conversation and answer participant questions about the protocol
• Schedule sessions, send reminders, chase no-shows and re-book them
• Log everything in our participant tracker and keep records audit-clean
• Report where the funnel is leaking so we can fix it
• Once trained, run study sessions yourself: device fitting, data collection, session notes

Who this is for

• No prior work experience required
• You spend most of the day on the phone with strangers
• You can get people to commit and follow through

Details

• $80,000/year
• 40 hours/week
• In person, Boston