Added
8 days ago
Type
Full time
Salary
Salary not provided

Related skills

informed consent regulatory submissions tmf ich-gcp regulatory compliance
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๐Ÿ“‹ Description

  • Delivery of site activation readiness for assigned sites
  • Prepare Clinical Trial Applications and submission dossiers
  • Interact with CA/EC and handle responses
  • Provide updates to Start Up Lead, Regulatory Lead, PM
  • Maintain project plans, trackers, and regulatory tools
  • Develop/start-up plans, IMP release requirements, essential reviews

๐ŸŽฏ Requirements

  • Bachelor in life sciences or RN or equivalent
  • Regulatory/start-up experience in CRO/pharma/biotech
  • Experience with CA/EC submissions and regulatory timelines
  • Romanian/Hungarian/English language for Romania is preferred
  • Strong communication and organizational skills
  • Fluency in English; IT systems and MS Office proficiency

๐ŸŽ Benefits

  • Remote work options for Hungary/ Romania region
  • Equal opportunity employer
  • Support for regulatory and site start-up career growth
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