Description

You will manage the configuration, customization, and support of the Veeva Vault CTMS platform.

Responsibilities

• Configure and customize Veeva Vault CTMS modules and workflows to support clinical trial processes.
• Collaborate with clinical operations, data management, and IT teams to ensure data integrity and system integration.
• Conduct system assessments to identify gaps and propose solutions for performance and compliance.
• Provide end-user support, troubleshooting, and issue resolution for CTMS functionality.
• Develop and maintain system documentation, including user guides, configuration guides, and SOPs.
• Lead user training and educational sessions to ensure effective platform utilization.

Required Skills

• 5+ years of experience working with Veeva Vault CTMS or similar clinical trial management systems.
• Proven experience configuring and customizing Veeva Vault CTMS modules, workflows, and reports.
• Deep understanding of clinical trial processes, including study startup, site management, and trial monitoring.
• Familiarity with regulatory requirements and guidelines such as ICH-GCP.
• Knowledge of data integration and system interoperability within the clinical trial ecosystem.
• Strong analytical skills for troubleshooting complex system-related issues.
• Bachelor's degree in Life Sciences, Computer Science, Information Systems, or a related field.

Preferred Skills

• Veeva Vault CTMS certification.
• Knowledge of EDC (Electronic Data Capture) or eTMF (electronic Trial Master File) systems.

Key Skills

Education

ANY GRADUATE