Thermo Fisher Scientific·12 days ago
12 days ago
Country Approval Specialist
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What you'll do
- Support the preparation and coordination of local regulatory submissions
- Ensure alignment with global strategies
- Manage submissions
- Provide local regulatory advice
- Support site start-up activities
What they're looking for
- Relevant experience in regulatory submissions and clinical trial site activation
- Strong communication skills
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
We are looking for a Country Approval Specialist to support the preparation and coordination of local regulatory submissions, ensuring alignment with global strategies. The role involves managing submissions, providing local regulatory advice, and supporting site start-up activities. Ideal for candidates with relevant experience and strong communication skills.
Skills
- regulatory submissions
- ethics committee submissions
- clinical trial site activation
- regulatory compliance review
- patient information sheet development
- informed consent form development
- ppd sops
- client sops
- medical terminology
- regulatory guidelines knowledge
- negotiation skills
- attention to detail
- planning skills
- computer skills
- english language proficiency
Company
Thermo Fisher Scientific
Remote, United Kingdom
Company facts come from this company's own listings. We only show what the postings themselves carry.