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About the role
Key responsibilities & impact- Monitor clinical trial sites through on‑site and remote visits
- Build and maintain strong relationships with investigators and site staff
- Collaborate with cross‑functional teams to meet project timelines
- Manage site‑level study documentation, systems updates, and visit reports
- Implement corrective actions when needed to maintain study integrity
- Ensure sites are always audit- and inspection-ready
Requirements
What you’ll need- Bachelor’s degree in life sciences, pharmacy, nursing, or related field is required
- A minimum of 1 year of CRA experience required
- Must be fluent in English and Portuguese
- Must be able to travel and hold a valid driver’s license
Benefits
Comp & perks- Enjoy work‑life balance and flexible working arrangements
- Unlock career growth and professional development opportunities
- Be part of groundbreaking projects pushing the boundaries of clinical research
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial monitoringsite-level study documentationcorrective actions implementation
Soft Skills
relationship buildingcollaborationproject management
