Senior Clinical Research Associate

📋 Description

• Lead start-up, site initiation and ongoing trial monitoring.
• Oversee site management to ensure patient safety and data quality.
• Mentor junior staff and provide training across teams.
• Coordinate regulatory submissions and investigator contracts.
• Prepare monitoring reports and ensure audit readiness.
• Travel 60-70% as needed.

🎯 Requirements

• Bachelor's degree or international equivalent.
• At least 3.5 years on-site monitoring experience.
• Global Clinical Trial experience.
• Proficient in MS Office (Outlook/Word/Excel/PowerPoint).
• Fluency in English (verbal and written).
• Travel required (60-70%).

🎁 Benefits

• Equal Opportunity Employer.
• Remote work environment.
• Opportunity to work in Oncology and Rare Disease.
• Training and mentorship for junior staff.