About this role
Clinical Affairs Project Manager at Robeauté. Location: France or Europe. Role: planning studies, coordinating trials, preparing documentation Requirements: MD/Masters/PhD or equivalent, 5+ years running preclinical (GLP) and early clinical device studies, IDE/regulatory submission experience preferred, device test experience, strong written communication. Category: Healthcare Services - Advanced Practice Seniority: Senior Level Commitment: Full Time Workplace: Remote Languages: English, French