Travel Clinical Research Coordinator
Core
Oversee and manage clinical operations at research sites, ensuring compliance with study protocols and regulatory guidelines while facilitating patient enrollment and study execution.
Role type
Traveling Clinical Research Coordinator
Builds
Clinical trials and patient data for pharmaceutical and biotech sponsors
Domain
Clinical research / Pharmaceutical Product Development
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery
Required skills
Clinical study management, GCP/ICH/FDA regulatory compliance, patient screening and consent, vital signs collection, data documentation, IRB coordination, adverse event reporting, site initiation meetings, team oversight, scheduling optimization
Preferred skills
English fluency, independent problem solving, negotiation, influencing, organizational skills, computer proficiency, interpersonal skills
Technologies
Computer generated forms, basic computer applications
Responsibilities
Conduct clinical studies according to FDA/GCP and ICH regulations; provide medical care to patients ensuring safety; schedule subject visits within protocol windows; perform study activities including informed consent, screening, vital signs, pregnancy tests, height, weight, ECGs, and blood samples; record patient information and test results; complete IP accountability logs; report suspected non-compliance; ensure IRB approval and requirements are met; promote the company and build positive relationships with patients; attend site initiation meetings; review study conduct plans; collect and document data accurately; monitor participant safety and well-being; serve as primary sponsor contact; ensure communications are documented; act as backup to direct people manager including overseeing work assignment, scheduling, monitoring time, interviewing, hiring, training, and mentoring team members
Seniority
Mid-level, hands-on IC with team oversight responsibilities
