🛠 Tech Stack

💼 About This Role

You'll join a global CRO supporting a dynamic biotech client in dermatology clinical trials. Your work ensures trial sites run smoothly and data integrity is maintained. This role offers the security of a large organization with the focus of a single sponsor.

🎯 What You'll Do

• Conduct site evaluation, initiation, and periodic monitoring visits.
• Train site staff on study procedures and protocols.
• Perform source data verification and review CRFs for accuracy.

📋 Requirements

• University degree in scientific, medical, or paramedical disciplines.
• Proven experience as a CRA with on-site monitoring.
• Previous experience in Dermatology studies.
• Strong knowledge of GCP/ICH guidelines.
• Fluent in English.

✨ Nice to Have

• Experience with contract negotiation and study budget.
• Familiarity with submission processes and informed consent development.

🎁 Benefits & Perks

• 🏖️ Flexible work arrangements
• 📚 Continuous training and career development
• 🌍 Global career opportunities

📨 Hiring Process

Estimated timeline: 1-2 weeks · AI estimate

1. 1Submit CV· 1 day
2. 2Phone Interview· 30 min