Manager, Global Clinical Solutions - UAT Team

AstraZeneca plc; Województwo mazowieckie; Hybrid; PLN 180,000 - 320,000; Full time

Job summary

The Manager, Global Clinical Solutions – UAT Team at AstraZeneca plc is based in Warsaw, operating a hybrid model with three days in the office. The role leads User Acceptance Testing quality, creates test plans and scripts, and oversees timely delivery within regulatory guidelines.

You will collaborate with global study teams and project vendors, mentor team members, and ensure testing documentation meets ICH GCP and SOX expectations while upholding AZ values.

Qualifications

• University degree in related discipline, preferably biological science or healthcare-related fields
• At least 2 year experience in Drug Development within a pharmaceutical or clinical background
• Understanding of clinical study and drug development processes and ICH GCP guidelines
• Ability to work collaboratively; proven organizational and analytical skills and delivery 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)
• AZ values and behaviors
• Some experience in Validation/User Acceptance Testing in a regulated environment with familiarity of Validation/Test Plans, Reports, Test scripts, etc.

Responsibilities

• Quality Lead – overall accountability for UAT (process, timelines and quality)
• Test Lead – create UAT documentation (Test Plan, Test Scripts, Test Report) and track testing issues
• Tester – responsible for executing Test Scripts

Skills

English proficiency

Communication skills

Analytical skills

Organizational skills

Collaborative work

Computer literacy

Education

Biological/healthcare field degree

2+ years drug development experience

Tools

Validation/Test Plans

Test Scripts

Job description

Manager, Global Clinical Solutions – UAT Team

Location: Warsaw

Hybrid model: 3 days per week from office in Warsaw

Global Clinical Solutions department (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.

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.

Date Posted 26-paź-2026

Closing Date 04-lis-2026