Clinical Research Spec
Medtronic · Tokyo, Japan +1 more
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Role summary
This clinical research specialist role supports trial safety and regulatory compliance across Japanese medical institutions. Responsibilities include monitoring clinical trials, managing site procedures, handling adverse events, and collaborating with internal and external stakeholders. The position requires 5+ years of monitoring experience at medical device or pharmaceutical companies and strong GCP knowledge.
Privacy & handoff
This role links to Medtronic's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.