Clinical Trial Administrator II

📋 Description

• Assists the project team with updating and maintaining clinical tracking systems.
• Prepares, handles, distributes, files and archives clinical documentation per SOPs.
• Stays abreast of regulatory/operational aspects relevant to assigned projects.
• Prepares and requests necessary local authorities' approvals.
• Oversees and manages agreements with hospitals and investigational centers.
• Collaborates on preparing, handling and distributing trial supplies and tracking.

🎯 Requirements

• High School Diploma or equivalent; college degree preferred.
• Three (3) years of clinical research experience in CRO/pharma.
• Knowledge of clinical trial operations, GCP/ICH Guidelines and regulatory requirements.
• Knowledge of English and local language(s).
• Proficiency in Microsoft Office (Word, Excel, Outlook).

🎁 Benefits

• Flexible Working Hours
• Full performance and development process with end of year reviews
• Team events and end of year party
• Employee satisfaction survey - your feedback is important for continuous improvement
• Health Insurance