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Thermo Fisher Scientific

Country Approval Associate

Thermo Fisher Scientific

. Prepare, review and coordinate Country Submissions under guidance and in alignment with global submission strategy .

Posted 10/15/2026full-timeRemote • BrazilJuniorMid-LevelWebsite

About the role

Key responsibilities & impact
  • Prepare, review and coordinate Country Submissions under guidance and in alignment with global submission strategy
  • Support preparation of local Ministry of Health submissions
  • Coordinate with internal functional departments on site start-up activities and submission timelines
  • Ensure submission processes align with the critical path for site activation
  • Achieve company target cycle times for sites
  • Contact investigators for submission-related activities as needed
  • Act as a country-level key contact for ethical or regulatory submission activities
  • Work with start-up CRAs to prepare regulatory compliance review packages
  • Assist in developing country-specific Patient Information Sheets and Informed Consent Forms
  • Assist with grant budgets and payment schedule negotiations with sites
  • Enter and maintain trial status information in tracking databases
  • Prepare, set up and maintain local country study files and filing processes
  • Maintain knowledge of PPD and client SOPs, directives and current regulatory guidelines

Requirements

What you’ll need
  • Bachelor's degree or equivalent and relevant formal academic / vocational qualification
  • Previous experience comparable to 0 to 2 years
  • Effective oral and written communication skills
  • Excellent interpersonal skills
  • Strong attention to detail and quality of documentation
  • Good negotiation skills
  • Good computer skills and ability to learn appropriate software
  • Good English language and grammar skills
  • Basic medical/therapeutic area and medical terminology knowledge
  • Ability to work in a team environment or independently, under direction, as required
  • Basic organizational and planning skills
  • Basic knowledge of applicable regional/national country regulatory guidelines and EC regulations
  • Equivalency may consist of appropriate education, training and/or directly related experience

Benefits

Comp & perks
  • Global team environment
  • Collaboration and development opportunities
  • Exposure to scientific innovation and excellence