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You will be updated with latest job alerts via emailAre you ready to dive into the world of clinical programming and make a difference in the lives of patients worldwide As a Clinical Programmer II youll be at the forefront of programming dashboard development and data validation for complex clinical studies. Collaborate with cross-functional teams and contribute to groundbreaking initiatives under the guidance of experienced programmers. Your expertise will help shape the future of healthcare!
Accountabilities:
In this dynamic role youll design develop implement and validate programs using SAS Python R SQL and dashboard applications like PowerBI and Spotfire. Your work will process analyze and report clinical trial data for review by study teams. Youll independently program with efficiency and quality contributing to medium to high complexity projects within the clinical programming roadmap. Collaborate with teams across data management development operations clinical biometrics and more to deliver end-user reporting needs. Develop and maintain data visualization tools automate manual checks reconcile data create operational reports and measure metrics for data cleaning status. Maintain a catalogue of reports and ensure their availability and performance for both external and internal users. Document programming tasks in compliance with SOPs and keep lead programmers updated on progress. Join us in implementing cross-functional projects that drive clinical programming forward!
Essential Skills/Experience:
- Bachelors degree or equivalent in computer science life science or statistics
- Good programming skills and prior experience in SAS/Python/R/SQL/Power BI/SpotFire and other dashboard technologies
- Basic knowledge of clinical development process
- Good dashboard development skill in PowerBI / Spotfire
- Basic knowledge on data capture data models data mining
- Excellent written and verbal communication skills
- Ability to work in a global team environment
- Good analytical skills and high attention to detail
Desirable Skills/Experience:
- Knowledge of industry standards
- Basic knowledge of FDA regulations and GCP/ICH guidelines as related to clinical programming processes
- Prior experience and understanding of EDC systems like Medidata Rave / Inform / Veeva/ Saama/ Entimice SAS LSAF etc.
- Knowledge on MicroStrategy
When we put unexpected teams in the same room we unleash bold thinking with the power to inspire life-changing -person working gives us the platform we need to connect work at pace and challenge perceptions. Thats why we work on average a minimum of three days per week from the office. But that doesnt mean were not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.
At AstraZeneca curiosity meets courage as we explore the possibilities of science to transform healthcare. Our inclusive environment fosters collaboration among the brightest minds from academia biotech and industry. By integrating data and technology with scientific innovation we aim to treat prevent modify and even cure complex diseases. With open doors and empowered voices we are committed to making a difference in patients lives globally.
Ready to take the next step in your career Apply now and be part of our journey to redefine whats possible in healthcare!
Date Posted
14-sept-2025Closing Date
13-sept-2025AstraZeneca 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.
Full-Time