Location: Warsaw Poland
Hybrid model of work: 3 days in office 2 remote per week
The Veeva Clinical Vault Business Analyst partners with Product Owners Engineering DevOps Architecture and Business stakeholders to design and deliver clinical capabilities across Veeva modules including eTMF CTMS Study Startup (SSU) Site ConnectExternallySponsoredResearchStudy Site Payments and Study Training. The role leads requirements elicitation business process design and solution evaluation to ensure high-quality compliant and value-driven outcomes aligned to AstraZeneca standards. This positionoperatesin agile teamsfacilitatesdiscovery and prioritization writes well-formed user stories and acceptance criteria and supports UAT and change management across global clinical stakeholders.
Typical Accountabilities
Agile Delivery:Build andmaintaineffective relationships with Product Owners/Managers Business Relationship Managers Enterprise Architects Developers Client Services and UX. Lead andfacilitatediscovery workshops to clarify scope and outcomes for new clinical capabilities. Write user stories scenarios and acceptance criteria using INVEST principles; manage and prioritize product backlogs; evangelize product roadmap; and provide demos and training on new features.
Business Needs Identification: Assess and define clinical business needs across Study Planning and Conduct TMF operations startup workflows site engagement payments and training. Proactivelyidentifyimprovement opportunities aligned with strategy substantiating proposals via research and benchmarking.
Business Analysis Planning: Selectappropriate analysisapproaches based on complexity risk assumptions constraints and dependencies. Plan and manage personal deliverables and deadlines; contribute to iteration planning and release readiness.
Stakeholder Analysis & Change:Identifyclinical and cross-functional stakeholders andmaintainrelationships tailored to influence and adoption needs. Contribute to communication and change plans that drive awareness readiness and sustained adoption across country affiliates CROs and sites.
Requirements & Design Definition:Own requirements management plans including elicitation approvals processes RAID and scope impacts. Maintain traceability through testing and validation. Translate business needs into design specifications spanning Functional Design User Interface considerations and Business Process Design. Partner closely with Architecture to ensure solutions deliver agreed benefits andcomply withdata privacyGxP and AZ quality standards.
Business Case & Benefits: Support business case development including investment rationale ROI measurable outcomes and benefits realizationplanfor clinical process efficiencies and quality improvements.
Solution Evaluation:Evaluate solution options for clinical readiness value forspending and operational impact. Provide recommendations grounded in data regulatory requirements and user experience feedback.
Veeva Clinical VaultKnowledge &Responsibilities
eTMF
CTMS
Study Startup (SSU)
Site Connect
Externally Sponsored ResearchStudy
Site Payments
Study Training
Collaboration
Collaborate with Business Relationship Managers Product Owners and Business Analysts to sustain strong business relationships enable process change and serve as a point of contact for application development and enhancements.
Partner with business customers& product ownerstoidentifyrequirements and communicate impacts costs and benefits; support and/or facilitate UAT planning test case design execution and defect triage.
Work with process owners to devise solutions that improve performance compliance and user experience across clinical operations and site interactions.
Coordinate with IT Architecture Delivery and Support to ensure clear requirements effective testing and high-quality releases that meet customer experience expectations.
Shared Responsibilities
Testing:Partner with Test Leads to define the testing approach traceability from requirements to test cases entry/exit criteria and coverage across functional integration UAT and regression testing.
Change & Communication:Partner with Change Management and Communication Leads to deliver stakeholder analysis communication plans training content and readiness activities to ensure adoption.
Essential
Practical experience with Agile methodologies (Scrum/Kanban) including backlog management and iterative delivery.
Hands-on use of business analysis tools and techniques to design and deliver business change in a regulated (GxP) environment.
Strong engagement communication facilitation and influencing skills; confident presenting to global stakeholders.
Experience working with third-party suppliers/CROs and cross-functional teams.
Demonstrated experience with Veeva Clinical Vault modules (eTMF CTMS SSU Site ConnectESRStudy Site Payments Study Training).
Ensure solutions align with AstraZeneca quality standardsGxPcontrols data privacy and audit readiness.
Maintain documentation integrity configuration control and change records to support inspections and internal audits.
Support periodic health checks and continuous improvement aligned to KPIs and benefits realization.
Delivery of prioritized backlog items to definition of done with high-quality acceptance outcomes.
Desirable
Degree in a relevant discipline and/or formal certification in business analysis (e.g. IIBA BCS) or Agile (e.g. CSMSAFe).
Experience working in a global pharmaceutical organization with awareness of clinical trial processes and regulatory frameworks (ICH-GCP GDPR).
Exposure to data governance master data and integration patterns across Veeva modules and enterprise systems.
Effective traceability from requirements through testing and release withtimelyclosure of RAID items.
Scripting knowledge Python or R
Date Posted
17-mar-2026Closing Date
26-mar-2026AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds with as wide a range of perspectives as possible and harnessing industry-leading skills. We believe that the more inclusive we are the better our work will be. We welcome and consider applications to join our team from all qualified candidates regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment) as well as work authorization and employment eligibility verification requirements.
Required Experience:
IC
AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, ... View more