{"id":3323403,"url":"https://alion.io/job/astrazeneca-manager-global-clinical-solutions-uat-team","title":"Manager, Global Clinical Solutions - UAT Team","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":92,"open_postings":156,"ghost_share":0.006,"stale_share":0.436,"repost_share":0.103,"time_to_fill_p50_days":19,"computed_at":"2026-10-31T05:58:55Z"}},"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":"structured","locations":["Warsaw, Poland"],"countries":["PL"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":17500,"max_usd":41000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":15},"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"Good Clinical Practice","optional":false}],"status":"live","first_seen_at":"2026-10-26T00:00:00Z","employer_posted_date":"2026-10-26","last_verified_at":"2026-10-31T19:44:14Z","board_verified":true,"closed_at":null,"days_open":5,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":5},"description":"Manager, Global Clinical Solutions - UAT Team\nLocation: Warsaw\nHybrid model: 3 days per week from office in Warsaw\nGlobal 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.\nThe GCS Manager - UAT Team is expected to be able to take the following roles within the team:\nQuality Lead - overall accountability for User Acceptance Testing (process, timelines and quality), review and approve of the documents \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 \nTester - responsible for Test Scripts execution \nThe team members will be cooperating with:\nGlobal Study Team representatives to clarify user requirements, scope of testing and intended system functionality; \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 \nAbility to work collaboratively; proven organizational and analytical skills, and proven skills to deliver to time, cost and quality \nComputer proficiency \nExcellent knowledge of spoken and written English \nStrong business communication and presentation skills \nAbility to transfer knowledge efficiently (mentorship/trainings) \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 \nDesirable qualifications:\nExpert reputation within AZ business area \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 \nSome experience in IRT/eCOA/ePRO/Spirometry/ECG solutions delivery \nSome experience of Quality Systems and Quality Management, including process definition and process improvement, ideally within an Information Systems environment \nAstraZeneca 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.\nDate Posted\n26-paź-2026Closing Date\n04-lis-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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