Clinical Research Associate I

📋 Description

• Oversees site management to protect patients and data quality.
• Guides audit readiness and regulatory submissions.
• Maintains trial management tools and status reports.
• Manages site start-up tasks: regulatory docs, consents.
• Conducts on-site and remote monitoring visits; reports findings.
• Supports recruitment, data entry, and tracking of study observations.

🎯 Requirements

• University degree in life sciences or healthcare field.
• Excellent communication and organizational skills; team player.
• Experience with computerized systems, spreadsheets, email.
• Able to travel up to 60% (international travel as needed).
• English fluency; local language as required by country.
• Oncology/EDC/EHR monitoring experience preferred.

🎁 Benefits

• Paid time off and volunteer time off.
• Comprehensive medical coverage.
• 401(k) plan with company match.
• Paid parental leave.
• Professional development opportunities.
• Work-life balance programs.