Business Analyst - Veeva Safety

Lokation: København

Job Description: We are looking for an experienced consultant to focusing on delivering Veeva Safety advanced business administration and support tasks that ensure operational excellence and compliance. This role requires a strong technical foundation, strategic thinking, and the ability to work independently while collaborating across various functions. Main Responsibilities: Lead and deliver complex business administration tasks related to Veeva Safety pharmacovigilance database operations and technology integrations, while supporting day-to-day operations, troubleshooting, and end-user support. Drive and support change implementation, including requirement clarification, impact and risk assessment, and execution of test cases with associated coordination. Ensure high-quality task execution to secure compliance with regulatory requirements and internal standards. Contribute to the development and continuous improvement of SOPs and training materials, collaborating with stakeholders to identify leaner working methods and proactively flag potential risks. Key Requirements: Deep knowledge of Veeva Safety database, including business administrator responsibilities, trial setup, data verification, and release support. Veeva CDMS and clinical trial design knowledge is a plus. Demonstrated ability to manage complex tasks with minimal guidance and deliver impactful results. Quality and compliance experience, including GxP validation documentation (e.g., User Acceptance Test plans), business testing, and regulatory compliance. Capable of developing training content and providing super-user support to global stakeholders. Nice to Have: Experience with pharmacovigilance systems and regulatory requirements. Strong analytical skills and problem-solving ability. Familiarity with project management methodologies. Start date: ASAP Duration: 12 months Location: Greater Copenhagen Area

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