Country Approval Associate

Prepare, review and coordinate local submissions in alignment with global submission strategy. Coordinate with internal departments to ensure site start-up activities align with submission timelines. Assist in developing country-specific Patient Information Sheet/Informed Consent form documents and maintain trial status information in tracking databases.

Bachelor's degree or equivalent and relevant formal academic/vocational qualification. Previous experience of 0 to 2 years in a related field. Effective oral and written communication skills, strong attention to detail, and basic knowledge of regulatory guidelines.

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