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Thermo Fisher Scientific·1 day ago
1 day agoBe an early applicant

Country Approval Specialist - FSP

Remote, PolandFull-timeRemoteMid · 2-5 years

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About this role

We are expanding our team: As a Country Approval Specialist, you will support the preparation and coordination of local regulatory submissions, ensuring alignment with global strategies. This role involves providing regulatory advice and managing site start-up activities. Ideal for candidates with relevant experience and strong communication skills.

Skills

  • regulatory submissions
  • ethics committee submissions
  • regulatory strategy
  • patient information sheet development
  • informed consent form development
  • regulatory compliance review
  • clinical trial site activation
  • trial status tracking
  • sop compliance
  • grant budget negotiation
  • feasibility coordination
  • medical terminology
  • regulatory guidelines knowledge
  • project coordination
  • negotiation
  • english language proficiency
  • teamwork
  • independent work
  • organizational skills
  • planning skills
H1B sponsor likely
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