Clinical Programmer I II

Job Title: Clinical Programmer I / II

Global Career Level: C

Role Type: Individual Contributor

Location: Manyata Tech Park Bangalore

Work Type: Hybrid

Experience: 2 to 6 years

About AstraZeneca:

AstraZeneca is a global science-led patient-focused pharmaceutical company that focuses on the discovery development and commercialization of prescription medicines targeting some of the planets most serious diseases. But were more than one of the worlds leading pharmaceutical companies. At AstraZeneca we re dedicated to being a Great Place to Work.

Introduction to role:

Are you ready to turn complex clinical data into clear actionable insights that sharpen study quality and speed confident decisions Do you want to build high-impact dashboards and programs that help teams spot issues early and elevate outcomes for patients As a Clinical Programmer II you will design and deliver data solutions that drive our clinical studies forward. You will focus on programming dashboard development and validation for ongoing trials of medium to high complexityhelping study teams see what matters sooner act faster and uphold the highest standards of data integrity.

Your work underpins the quality of our evidence and the reliability of our conclusions. You will join a collaborative cross-functional environment where science and technology meets. Partnering with clinical data management biometrics and operations you will translate real user needs into robust tools and visualizations. Guided by experienced programmers youll own well-defined scope build within proven frameworks and contribute to a roadmap that advances how we run trials across critical disease areas.

Accountabilities:

Clinical Data Programming: Design develop implement and validate programs in SAS Python R and SQL to process analyze and report clinical trial data ensuring timely high-quality outputs for clinical study teams.

Dashboard Development: Build validate and maintain Power BI Spotfire and MicroStrategy dashboards from requirements gathering and data provisioning to design testing training and performance support for internal and external users.

Automation and Data Quality: Create and maintain a catalog of reports to aid data cleaning; automate manual checks; program reconciliation and edit checks for TPV data; build tools and repositories to reduce data errors at source including lab reference ranges.

Operational Reporting: Program operational reports such as missing pages open/closed queries PI signatures and audit trail outputs; detect subject-level errors and deliver metrics that track data cleaning status and study readiness.

Discrepancy Detection and Visualization: Develop visualizations and dashboards that highlight discrepancies between EDC and TPV data enabling proactive issue resolution by study teams.

Frameworks Quality and Documentation: Work within established frameworks and SOPs; embed quality in all deliverables; complete documentation including peer reviews and report specifications; maintain and update assets as requirements evolve.

Independent Delivery and Progress Updates: Complete tasks independently within a well-defined scope; communicate progress and risks to lead programmers; ensure availability and performance of reports and dashboards.

Roadmap Contributions and Collaboration: Contribute to medium to high complexity initiatives on the clinical programming roadmap; collaborate with data management development operations clinical biometrics and other teams to deliver on end-user reporting needs and cross-functional projects.

Essential Skills/Experience:

Bachelors/Masters 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 distributed 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 the 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.

Why AstraZeneca:

Here science meets technology to solve real problems for patients. You will join a bold fast-moving environment where unexpected teams come together to spark bold thinkingfrom evidence generation and clinical trials to digital solutions that connect the entire care journey. We are advancing a growing pipeline and reimagining how data can speed launches and elevate outcomes all while valuing kindness alongside ambition. You will have the support trust and autonomy to take smart risks learn rapidly and see your work translate into better decisions and better health for people worldwide.

Call to Action:

Step into a role where your code curiosity and leadership will shape smarter trials and better patient outcomes.

Date Posted

Closing Date

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.