Statistical Programmer II

Job Title: Statistical Programmer II

Introduction to role

Are you ready to make a difference in the world of biopharmaceuticals? As a Statistical Programmer II, you'll play a crucial role in developing and validating programs that create datasets conforming to Alexion and CDISC standards. You'll be responsible for generating Tables, Listings, and Figures for analysis purposes, ensuring adherence to ICH guidelines, Good Clinical Practices, and regulatory requirements. This position offers the opportunity to work on moderate scope and medium complexity studies or drug projects, contributing to continuous improvement within cross-functional teams. Under the guidance of an experienced programmer, you'll enhance your understanding of statistical concepts and SAS Programming while making a meaningful impact.

Accountabilities

• Support the development of technical programming specifications for SDTM, ADS, or ADaM standards under guidance.
• Develop and validate programs that generate SDTM datasets, analysis datasets, and tables, listings, figures/graphs based on Protocol and SAP.
• Understand protocols and clinical development plans to contribute effectively.
• Ensure high quality in deliverables within established frameworks.
• Work independently on well-defined tasks.
• Acquire knowledge of the drug development process and industry standards.
• Increase proficiency in SAS and other statistical computing software.
• Collaborate with clinical study teams and other functions in drug development.
• Keep the lead programmer updated on progress.
• Collaborate with external vendors and contract programmers.
• Provide updates on programming activities.
• Support project leadership in implementing department standards.
• Contribute ideas for optimizing standard operating procedures.

Essential Skills/Experience

• 2 to 4 years of statistical programming experience in the Pharmaceutical, Biotechnology, or Contract Research Industry.

Desirable Skills/Experience

• Understand the concepts of development and validation of technical specifications and programs for safety and efficacy analysis datasets, tables, listings, and figures/graphs.
• Work collaboratively to resolve problems.
• Clearly communicate with management and team members.
• Understanding and basic competence in using SAS/Base, SAS/Macro, SAS/STAT, or other statistical computing software.
• Basic understanding of relational databases and good programming practices.

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're 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, you'll find an environment where innovation thrives! Our commitment to patients drives us to push boundaries and redefine possibilities. With a rapidly expanding portfolio, you'll have the chance to grow and innovate alongside passionate colleagues. Our culture fosters connections, encourages new ideas, and supports your career journey. Here, your work is more than just a job—it's a chance to make a real impact on patients' lives.

Ready to take the next step? Apply now and be part of something extraordinary!