FSP Bench Country Approval Specialist
Thermo Fisher Scientific · Santiago, Chile
QualityFull timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Country Approval Specialist role supporting clinical trial regulatory submissions across multiple jurisdictions. Responsible for preparing and coordinating local regulatory submissions, providing strategic guidance, and ensuring alignment with global submission timelines in an office-based environment.
What they're looking for
- Bachelor's degree or equivalent formal qualification
- 2+ years relevant experience in regulatory or clinical trial operations
- Strong written and oral communication skills in English
- Basic knowledge of regional and national regulatory guidelines
- Proficiency with computer systems and software applications
- Attention to detail and quality documentation standards
- Negotiation and interpersonal skills
What you'll be doing
- Prepare, review, and coordinate local regulatory submissions aligned with global strategy
- Provide regulatory and strategy advice to internal clients at country level
- Coordinate site start-up activities and ensure submission process alignment
- Maintain trial status information in tracking databases accurately and timely
- Develop country-specific patient information and informed consent documents as needed
Privacy & handoff
This role links to Thermo Fisher Scientific's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.