{"id":1189315,"url":"https://alion.io/job/astrazeneca-manager-global-clinical-solutions-uat-team-secondment","title":"Manager, Global Clinical Solutions - UAT Team (secondment)","company":{"id":13195,"name":"AstraZeneca","domain":"astrazeneca.com","url":"https://alion.io/company/astra-zeneca","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"A","score":94,"open_postings":190,"ghost_share":0,"stale_share":0.421,"repost_share":0.053,"time_to_fill_p50_days":14,"computed_at":"2026-10-17T05:46:00Z"}},"role":"Sales","role_family":"Sales","seniority":"junior","employment_type":"full_time","work_mode":"hybrid","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"explicit","locations":["Warsaw, Poland"],"countries":["PL"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false}],"status":"closed","first_seen_at":"2026-09-24T15:37:34Z","employer_posted_date":"2026-09-24","last_verified_at":"2026-09-30T04:50:27Z","board_verified":false,"closed_at":"2026-09-30T04:50:27Z","days_open":5,"trust":{"level":"not_scored","repost_count":null,"flags":[],"days_open":5},"description":"Job Title: Manager, Global Clinical Solutions (UAT - User Acceptance Testing)\nLocation: Warsaw, Poland\nWork model: Hybrid (3 days per week in office)\nGlobal Clinical Solutions department (GCS) drives the delivery of Business Process Excellence and Technology for the Clinical Operations organization, owning and providing industry leading process, technology and services on behalf of Clinical Operations and its internal and external Partnerships.\nThe Test Lead in UAT Team (testing of IRT/RTSM solutions) is expected to be able to take the following roles within the team in line with their growing expertise:\nTester - responsible for Test Scripts execution (during onboarding phase)\nTest 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.\nQuality Lead - overall accountability for User Acceptance Testing (process, timelines and quality), review and approve of the documents (typically TL grows into the QL role within 1 year of gaining TL experience)\nundefined\nThe Test Lead will be cooperating with:\nGlobal Study Team representatives to clarify user requirements, scope of testing and intended system functionality;\nSupply Chain Study Managers to receive input to the testing documentation\nVendor Representatives (Project Managers) to set testing pre-requisites and work on testing issues\nEssential qualifications:\nUniversity 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\nAt least 2 year experience in Drug Development within a pharmaceutical or clinical background\nUnderstanding of the clinical study and drug development process and ICH GCP guidelines in relation to study delivery operational activities\nProject Management and stakeholder management skillsAbility to work collaboratively; proven organizational and analytical skills, and proven skills to deliver to time, cost and quality\nAbility to proactively identify risks and issues as well as possible solutions \nStrong time management and prioritisation skills\nStrong business communication and presentation skills\nAbility to transfer knowledge efficiently (mentorship/trainings)\nExcellent knowledge of spoken and written English\nExhibit of AZ Values and Behaviours\nSome 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\nSome experience in working with IRT/RTSM solutions\nDesirable qualifications:\nSome experience of Quality Systems and Quality Management, including process definition and process improvement, ideally within an Information Systems environment\nExperience of utilizing standard process improvement methodologies (e.g. Lean Six Sigma) to identify root causes of process issues and identify areas of process improvement\nExperience in the development and management of Business Process to deliver business performance\nComprehensive knowledge of ICH GCP\nWhat we offer:\nWelcome to Warsaw Site, one of over 400 sites here at AstraZeneca, providing a collaborative environment where everyone feels comfortable and able to be themselves is at the core of AstraZeneca’s priorities, it’s important to us that you bring your full self to work every day.\nTo help you maintain your best self, here’s a sneak peek into some of the things this site provides for you:\nThe best team to support you,\nMultisport card,\nPension plan,\nLife insurance,\nafter-work events,\nprivate medical care\nlunch card,\nbright and spacious environment,\nsustainable office working environment.\nPlease note that we are working in a hybrid model of 3 days per week from the office in Warsaw\nDate Posted\n24-wrz-2026Closing Date\n29-wrz-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. 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