Clinical Trial Associate

• Support the Regional Clinical Study Manager in regional study delivery and delegated clinical study components
• Support Clinical Research Associates and Study Start-up Specialists in country study delivery
• Support clinical trial conduct, including feasibility assessment, study start-up, document generation and review, sample tracking, and participant enrollment
• Support CTMS updates, ISF binder preparation, document collection, ICF customization, and eTMF maintenance
• Interpret and implement regulations and ICH guidelines
• Set up regional and country team meetings, agendas, and minutes
• Maintain SharePoint folders, distribution lists, eTMF, CTMS, and other study systems
• Support system access requests and user account management
• Support study start-up, investigator meetings, TMF creation, review, and quality control
• Help resolve regional or country clinical supply issues and support data cleaning
• Prepare site newsletters and clinical trial correspondence
• Support public registry information maintenance and Clinical Study Report inputs
• Support operational risk identification, audits, inspections, tools, work instructions, and SOPs
• Support vendor setup, regional study budgets, purchase orders, payments follow-up, and accrual activities

Explore Regional Clinical Trial Management Associate at BeOne Medicines. Review requirements and application details.

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