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

Warsaw, Masovian Voivodeship, Poland -

Full Time

Start Date

Immediate

Expiry Date

30 May, 26

Salary

0.0

Posted On

01 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. AstraZeneca is a global, science-led, patient-focused biopharmaceutical company. We focus on discovering, developing and commercialising prescription medicines for some of the world’s most serious diseases. But we are more than one of the world’s leading pharmaceutical companies. At AstraZeneca, we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science, challenge convention and unleash your entrepreneurial spirit. To embrace differences and take bold actions to drive the change needed to meet global healthcare and sustainability challenges. There is no better place to make a difference in medicine, patients, and society. An inclusive culture where you will connect different thinking to generate new and valuable opportunities. Where you will find a commitment to lifelong learning, growth and development for all. Our Inclusion & Diversity (I&D) mission is to create an inclusive and equitable environment where people belong, using the power of our diversity to push the boundaries of science to deliver life-changing medicines to patients. Inclusion and diversity are fundamental to the success of our company, because innovation requires breakthrough ideas that only come from a diverse workforce empowered to challenge conventional thinking. We’re curious about science and the advancement of knowledge. We find creative ways to approach new challenges. We’re driven to make the right choices and be accountable for our actions. As an organisation centred around what makes us human, we put a big focus on people. Across our business, we want colleagues to wake up excited about their day at the office, in the field, or in the lab. Along with our purpose to bring life-changing medicines to people across the globe, we have a promise to you: to help you realise the full breadth of your potential. Here, you’ll do work that has the potential to change your life and improve countless others. And, together with your team, you’ll shape a culture that unites and inspires us every day. This is your life at AstraZeneca.

Responsibilities

Interns will contribute to meaningful projects within the TRIal Safety Data Review Centre (TRISARC) Technical Team, focusing on enhancing safety data review across therapeutic areas. This involves delivering modern, compliant GxP solutions, including analyses, visualizations, and applications supporting Clinical Trial Safety.