Manager, Global Clinical Solutions - UAT Team

AstraZeneca plc; Warszawa; Hybride; PLN 150 000 - 210 000; Plein temps

Résumé du poste

AstraZeneca plc is seeking a Manager, Global Clinical Solutions – UAT Team in Warsaw. This hybrid role combines quality leadership, test planning and execution to ensure timely, high-quality UAT delivery for complex clinical systems.

The successful candidate will oversee UAT documentation, coordinate with global study teams and vendors, and mentor teammates while maintaining alignment with GCP, regulatory standards and AZ values in a dynamic pharmaceutical environment.

Qualifications

• University degree in biological sciences or healthcare-related field or equivalent.
• At least 2 years experience in Drug Development in pharma/clinical setting.
• Understanding of ICH GCP guidelines in relation to study delivery operational activities.
• Excellent English and strong written/spoken communication.
• Experience in UAT and testing documentation (Test Plan, Test Scripts, Test Report).
• Experience with validated computerised systems in regulated environments (GxP, SOX).
• Demonstrated mentoring and knowledge transfer capabilities.

Responsabilités

• Quality Lead for UAT process, timelines and overall quality.
• Test Lead responsible for creating UAT docs (Plan, Scripts, Report) and tracking issues.
• Tester responsible for executing Test Scripts.

Connaissances

English proficiency

Quality leadership

Test documentation

Test execution

Communication skills

Mentorship

Team collaboration

Time/cost/quality delivery

Formation

University degree in biological sciences or healthcare

Outils

Validation/Testing documentation tools

Description du poste

Manager, Global Clinical Solutions – UAT Team

Location: Warsaw

Hybrid model: 3 days per week from office in Warsaw

Global Clinical Solutionsdepartment (GCS) drives the delivery of Business Process Excellence and Technology for the Clinical Operations organization, owning and providing industry leading processes, technology and services on behalf of Clinical Operations and its internal and external Partnerships.

The GCS Manager – UAT Team is expected to be able to take the following roles within the team:

• Quality Lead – overall accountability for User Acceptance Testing (process, timelines and quality), review and approve of the documents
• Test Lead – responsible for creating User Acceptance Testing documentation (Test Plan, Test Scripts, Test Report), review of the User Requirement Specification (to understand testing requirements) and tracking testing issues
• Tester – responsible for Test Scripts execution

The team members will be cooperating with:

• Global Study Team representatives to clarify user requirements, scope of testing and intended system functionality;
• Vendor Representatives (Project Managers) to set testing pre-requisites and work on testing issues

Essential qualifications:

• University degree in related discipline, preferably in biological science or healthcare-related fields, such as medicine, nursing or sanitary engineering, or equivalent experience in the aforementioned disciplines
• At least 2 year experience in Drug Development within a pharmaceutical or clinical background
• Understanding of the clinical study and drug development process and ICH GCP guidelines in relation to study delivery operational activities
• Ability to work collaboratively; proven organizational and analytical skills, and proven skills to deliver to time, cost and quality
• Computer proficiency
• Excellent knowledge of spoken and written English
• Strong business communication and presentation skills
• Ability to transfer knowledge efficiently (mentorship/trainings)
• Exhibit of AZ Values and Behaviours
• Some experience in Validation/User Acceptance Testing of computerised systems in a regulated environment, preferably the Pharmaceutical industry, including familiarity with documentation such as Validation/Test Plans, Reports, Test scripts (including test scripts execution), Functional Risk Assessment etc. and knowledge of regulatory (GxP, SOX etc.) requirements for computerised systems and infrastructure

Desirable qualifications:

• Expert reputation within AZ business area
• Experience of utilizing standard process improvement methodologies (e.g. Lean Six Sigma) to identify root causes of process issues and identify areas of process improvement
• Experience in the development and management of Business Process to deliver business performance
• Comprehensive knowledge of ICH GCP
• Some experience in IRT/eCOA/ePRO/Spirometry/ECG solutions delivery
• Some experience of Quality Systems and Quality Management, including process definition and process improvement, ideally within an Information Systems environment

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, gender identity or re‑assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised.

Date Posted 26-paź-2026

Closing Date 04-lis-2026

AstraZeneca 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.