Thermo Fisher Scientific·3 months ago
3 months ago
Country Approval Specialist - FSP
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About this role
Become part of our team as a Country Approval Specialist, supporting the preparation and coordination of local regulatory submissions for clinical trials. You will collaborate with internal and external partners to ensure timely site activation and document accuracy. Ideal for candidates with experience in the pharmaceutical industry and strong organisational and communication skills.
Skills
- regulatory submissions
- clinical trial agreements
- fda guidelines
- ich-gcp guidelines
- clinical development
- pharmaceutical industry knowledge
- budgeting
- fair market value principles
- medical terminology
- negotiation skills
- attention to detail
- computer skills
- english language proficiency
- planning skills
- site performance metrics
- document review
- site activation
- clinical operations
- regulatory guidelines knowledge
Company
Thermo Fisher Scientific
Remote, United Kingdom
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