Veeva CTMS Specialist — Clinical Systems Analyst

Amgen Inc.; Portugal; Presencial; EUR 50.000 - 68.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible work arrangements

Descripción de la vacante

Amgen Capability Center Portugal in Lisbon seeks a Clinical Systems Business Analyst to support CTMME and Veeva ClinOps, bridging business needs with technical delivery. You will gather requirements, write user stories, and craft test plans, collaborating with developers, Product Managers, and stakeholders to ensure aligned, high-quality solutions.

You will help source data, ensure regulatory alignment, and validate implementation while contributing to continuous improvement and effective

Formación

• Must hold a Doctorate or Master’s degree with 4–6 years of IT/Computer Science experience, or a Bachelor’s with 6–8 years experience, or a Diploma with 10–12 years experience.
• Proven experience with SAFe framework and Agile software development.
• Experience with Veeva ClinOps suite of applications and regulatory-aware data handling.

Responsabilidades

• Collaborate with System Architects and Product Managers to manage business analysis activities.
• Lead activities to capture the voice of the customer and define business processes and product needs.
• Develop business cases to request funds for digital innovation opportunities, including scope, timeline, and resources.
• Collaborate with Product Management and partners to analyze impact of Veeva version upgrades and refine the Product backlog.
• Ensure non-functional requirements are included and prioritized in product and release backlogs.
• Express features clearly in user stories so the team understands how they fit the backlog.

Conocimientos

SAFe

Veeva ClinOps

Jira

Agile methodologies

Communication

Educación

Doctorate degree

Master’s degree

Bachelor’s degree

Diploma

Herramientas

Jira Align

CI/CD tools

Descripción del empleo

Amgen Capability Center Portugal in Lisbon seeks a Clinical Systems Business Analyst to support CTMME and Veeva ClinOps, bridging business needs with technical delivery. You will gather requirements, write user stories, and craft test plans, collaborating with developers, Product Managers, and stakeholders to ensure aligned, high-quality solutions.

You will help source data, ensure regulatory alignment, and validate implementation while contributing to continuous improvement and effective