UAT Lead, Global Clinical Solutions

AstraZeneca plc; Warszawa; Hybrid; PLN 180,000 - 240,000; Full time

Benefits offered by this job

Multisport card

Pension plan

Life insurance

After-work events

Private medical care

Lunch card

Bright, spacious environment

Sustainable office

Job summary

AstraZeneca plc in Warsaw, Poland is seeking a Manager for Global Clinical Solutions with UAT leadership responsibilities. The role focuses on testing IRT/RTSM solutions, creating UAT documentation, and ensuring timely, high-quality delivery within a hybrid work model.

The ideal candidate has a biology/healthcare degree, 2+ years in drug development, strong English, and experience with validation testing in regulated environments. Collaboration with cross-functional teams is essential.

Qualifications

• University degree in biology/healthcare or related field.
• At least 2 years in Drug Development within pharma/clinical settings.
• Understanding of clinical study and ICH GCP guidelines.
• Project and stakeholder management skills; ability to deliver on time and budget.
• Strong English language skills (spoken and written).
• Experience with Validation/UAT of computerised systems in regulated environments.
• Experience with IRT/RTSM solutions.

Responsibilities

• Tester – execute Test Scripts during onboarding phase.
• Test Lead – create UAT documentation (Test Plan, Test Scripts, Test Report) and track issues.
• Quality Lead – own UAT process, timelines and quality; document reviews.
• Collaborate with Global Study Team, Supply Chain Study Managers and Vendors.

Skills

Test Leadership

Stakeholder management

Time management

Mentorship

English proficiency

Education

University degree

Job description

AstraZeneca plc in Warsaw, Poland is seeking a Manager for Global Clinical Solutions with UAT leadership responsibilities. The role focuses on testing IRT/RTSM solutions, creating UAT documentation, and ensuring timely, high-quality delivery within a hybrid work model.

The ideal candidate has a biology/healthcare degree, 2+ years in drug development, strong English, and experience with validation testing in regulated environments. Collaboration with cross-functional teams is essential.