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SSU CRA 2

ICON · Mexico City, Mexico

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Clinical OperationsFull-timeCompany career page

RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.

Role summary

Study Start-Up CRA II role overseeing site activation and clinical trial initiation in Mexico City. Responsible for managing site start-up activities, regulatory submissions, and ensuring compliance with local regulations and ICH-GCP guidelines while maintaining stakeholder relationships.

What they're looking for

  • Bachelor's degree in scientific or healthcare-related field
  • Strong experience in study start-up and site activation within CRO or clinical research organization
  • Prior Clinical Research Associate monitoring experience and site management knowledge
  • Comprehensive knowledge of ICH-GCP, Ethics Committee processes, and essential document management
  • Current understanding of COFEPRIS regulations and recent Mexican regulatory changes
  • Ability to manage multiple sites and projects with strong organizational skills
  • Experience with clinical trial management systems and eTMF platforms

What you'll be doing

  • Oversee site start-up and activation activities aligned with study timelines and sponsor expectations
  • Prepare and coordinate regulatory submissions to Ethics Committees and authorities per local requirements
  • Ensure compliance with current Mexican regulations and recent COFEPRIS requirements
  • Collect, review, and maintain regulatory documentation for site activation with investigative sites
  • Identify and resolve start-up challenges collaborating with cross-functional teams

Privacy & handoff

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What RoleLantern checked

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Date posted4 days ago
Last source checkToday
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