Visualization Developer Intern - Working in Science 2026 Internship Program at AstraZeneca

Warsaw, Masovian Voivodeship, Poland -

Full Time

Start Date

Immediate

Expiry Date

31 May, 26

Salary

0.0

Posted On

02 Mar, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Attention To Detail, Analytical Thinking, Data Analysis, Programming, Python, R, SAS, Power BI, Data Visualization, Relational Databases, SQL, Requirements Gathering, Business Analysis

Industry

Pharmaceutical Manufacturing

Description

Visualization Developer Intern - Working in Science 2026 Internship Program Turn your curiosity into impact. Join AstraZeneca for a 3 – month hybrid internship starting in July and work with teams pushing the boundaries of science. About the program The Working in Science Internship Program is designed for last year's students and recent graduates who want to apply what they’ve learned in a real, global biotechnology environment. You’ll contribute to meaningful projects, gain mentorship, and develop skills that set you up for future success. Department description: TRISARC Technical Team The TRIal Safety Data Review Centre (TRISARC) is a global centre that conducts first‑line reviews of important, pre‑specified safety data in late‑phase clinical trials. The TRISARC Technical Team enables and enhances safety data review across all therapeutic areas by delivering modern, compliant GxP solutions - including analyses, visualizations, and applications. The team is responsible for tool configuration, scripting, and data analysis activities that support Clinical Trial Safety. Required skills, candidate background: Strong attention to detail & analytical thinking Able to accurately review complex information and summarize key insights. Relevant background: Life sciences, bioinformatics, information technology, or a related field. Data analysis/programming: Experience with Python, R, SAS, and/or Power BI for data analysis or data mining. Data skills: Data cleaning, visualization, and working with relational databases (e.g., SQL). Requirements gathering: Comfortable capturing stakeholder needs and translating them into clear requirements. Business analysis: Ability to structure problems, interpret findings, and communicate recommendations. Key details Eligibility: Final year students and recent graduates. Please review the specific requirements for each role. Duration: 3 months, starting in July. Working model: Hybrid, with partial on‑site presence. Selection process: Application review against objective criteria, HireVue video responses, then a remote meeting with the recruiting team. Timeline: Apply by 21 March 2026. Results by mid-April. Important information Completion of the internship does not guarantee contract extension or further employment at AstraZeneca. Future opportunities may be advertised separately and require a new application. How to apply Read the role description carefully and submit your application before the deadline. Shortlisted candidates will receive an invitation to complete HireVue. You can also connect with our community and learn more about the program via our LinkedIn group: https://qr.short.az/Join_our_LinkedInGroup Date Posted 01-mar-2026 Closing Date 21-mar-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.

Responsibilities

Interns will contribute to meaningful projects within the TRIal Safety Data Review Centre (TRISARC) Technical Team, which enhances safety data review across therapeutic areas by delivering modern, compliant GxP solutions. This includes supporting Clinical Trial Safety through tool configuration, scripting, and data analysis activities.