Veeva Vault Solution Architect – Clinical, Regulatory, Quality Systems

This is a fully remote position, open to applicants in United States.

📋 Description

• Act as the technical expert for Veeva Clinical, RIM, and Quality applications.

• Establish solution architecture, configuration standards, integration patterns, and technical governance for the Veeva Vault platform.

• Collect and assess business, technical, data, security, and regulatory requirements, converting them into scalable solution designs.

• Facilitate requirements workshops, architecture discussions, design evaluations, and technical decision-making with both business and technology stakeholders.

• Create and manage integrations between Veeva Vault and clinical, regulatory, quality, enterprise, and data platforms.

• Provide technical guidance for system implementations, enhancements, upgrades, releases, and application lifecycle activities.

• Collaborate with development and implementation teams to evaluate technical designs, APIs, data mappings, migration strategies, and custom components.

• Suggest the optimal use of standard Veeva features to reduce unnecessary customization and enhance maintainability.

• Assist with Computer Software Assurance and Computer System Validation activities, including risk evaluations, validation planning, testing, traceability, and change control.

• Ensure solutions comply with relevant requirements, including GxP, 21 CFR Part 11, EU Annex 11, data integrity, security, privacy, records retention, and audit trail mandates.

⛳️ Requirements

• Bachelor’s degree in Information Technology, Computer Science, Engineering, Life Sciences, or a related field.

• Minimum of 5 years of experience in implementing, architecting, or supporting Veeva Vault solutions within the pharmaceutical, biotechnology, medical device, or life sciences sectors.

• In-depth knowledge of Veeva Vault architecture, configuration, security, workflows, object models, reporting, APIs, and integration functionalities.

• Active Veeva certification or proven implementation experience in relevant Veeva applications is highly preferred.

• Familiarity with GxP, FDA regulations, 21 CFR Part 11, EU Annex 11, and applicable data integrity standards.

• Capability to juggle multiple priorities and collaborate effectively across business, technical, and vendor teams in a dynamic environment.

🏝️ Benefits

• None specified