Remote Veeva Vault Administrator for GxP Compliance

TFS HealthScience; Lisboa; Presencial; EUR 60 000 - 90 000; Tempo integral

Resumo da oferta

TFS HealthScience is seeking a Veeva Vault Administrator to ensure reliable operation, configuration, and continuous improvement of the Veeva Vault platform across regulated environments. This home-based Europe role partners with IT and business users to translate needs into scalable solutions that support Quality, Clinical, and Regulatory workflows.

You will configure workflows, manage permissions, support quarterly releases, and maintain data integrity with IQ/OQ/PQ validation.

Qualificações

• 4+ years of experience administering Veeva Vault (CLINICAL OPERATIONS) or similar CMS.
• Certified in Veeva Vault.
• Strong understanding of document management in regulated industries.

Responsabilidades

• Administer and configure Veeva Vault applications (CTMS, eTMF, RIM).
• Configure workflows, lifecycles, security, and metadata.
• Manage user roles, permissions, and access controls.
• Provide end-user support and deliver training materials.
• Support quarterly releases, testing, and deployment.
• Coordinate validation activities in regulated environments.
• Ensure system compliance with GxP and regulatory standards.
• Maintain audit trails and data integrity.
• Oversee document lifecycle management and data migrations.
• Collaborate with IT for integrations and troubleshooting.
• Develop and maintain reports and dashboards.

Conhecimentos

Veeva Vault

System Administration

Regulatory Compliance

Training & Support

Formação académica

Bachelor’s degree in IT or Life Sciences

Ferramentas

Veeva Vault (CTMS/eTMF/RIM)

Descrição da oferta de emprego

TFS HealthScience is seeking a Veeva Vault Administrator to ensure reliable operation, configuration, and continuous improvement of the Veeva Vault platform across regulated environments. This home-based Europe role partners with IT and business users to translate needs into scalable solutions that support Quality, Clinical, and Regulatory workflows.

You will configure workflows, manage permissions, support quarterly releases, and maintain data integrity with IQ/OQ/PQ validation.