Clinical Trial Associate

A global clinical research team is seeking a Clinical Trial Associate (CTA) to support the coordination, documentation, and compliance of clinical trials. This role ensures trials are conducted efficiently and in accordance with GCP standards.

Key Responsibilities

• Support Clinical Trial Managers with trial logistics and documentation
• Maintain and review Trial Master File (eTMF) records
• Organize trial meetings and take minutes
• Manage system access and support team training
• Assist with vendor oversight, submission packages, and reporting
• Provide administrative support to leadership and department initiatives

Qualifications

• Bachelor’s degree or equivalent experience in life sciences
• Minimum 1 year in clinical operations or related field
• Familiar with ICH-GCP and TMF structure (DIA model)
• Proficient in Microsoft Office and at least one clinical trial system
• Strong communication and organizational skills