Statistical Programmer II

The Senior Statistical Programmer will be a primary resource for the development and validation of programs which create datasets conforming to Alexion and CDISC standards, as well as Tables, Listings, and Figures (“TLFs”) for analysis purposes. You will develop specifications to ensure that statistical programming elements align with the overall deliverable and adhere to ICH guidelines, Good Clinical Practices, and regulatory requirements. Supporting the Programming Lead, you may represent Statistical Programming in meetings with internal and external clients and cross-functional project teams. As a mentor to Statistical Programmers and Associate Statistical Programmers, you must demonstrate a strong ability to integrate statistical concepts with SAS Programming efficiently and effectively.

Accountabilities:
- Support development of technical programming specifications for SDTM, ADS or ADaM standards.
- Independently develop and/or validate programs that generate SDTM and analysis datasets based on Alexion or ADaM specifications.
- Support development and validate technical programming specifications for tables, listings, figures/graphs based on Protocol and SAP.
- Independently develop and validate programs that generate tables, listings, figures/graphs using Alexion specifications.
- Manage external vendors and contract programmers.
- Provide project progress updates of programming activities.
- Review, maintain, and approve protocol-specific documents as necessary.
- Provide guidance and mentoring to peer, junior-level Programmers and contract staff.
- Support project leadership ensuring that department standards are implemented in all studies.
- Contribute ideas and thoughts towards the optimization of standard operating procedures.
- Lead team meetings when appropriate.
- Any other activities as required.

Essential Skills/Experience:
- Minimum of 4 years of statistical programming experience in the Pharmaceutical, Biotechnology, or Contract Research Industry.
- Proven ability to:
  - Develop and validate technical specifications and programs for safety and efficacy analysis datasets, tables, listings, and figures/graphs.
  - Independently and collaboratively resolve problems.
  - Clearly communicate processes and standards with management and team members.
- High competence in using SAS/Base, SAS/Macro, SAS/STAT.
- Knowledge of SAS/Graph, and SAS/SQL.
- Knowledge and implementation of:
- SDTM and ADaM principles.
- Relational Databases.
- Good Clinical Practice principles.
- Good Programming Practice principles.
- 21CFR Part 11 Standards principles.
- Integrated Summary Safety/Efficacy Analyses.
- Safety data and Coding Dictionaries (MedDRA and WHODD).
- ICH eCTD format.

Desirable Skills/Experience:

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, we champion diversity in a patient-driven, energizing culture where people build connections to explore new ideas that profoundly impact patients' lives. Here, diversity and different thinking are valued, so life-changing new ideas can come from everywhere. We celebrate and reward each other, ensuring kindness remains as important as our ambition to succeed for those in need. We take pride in giving back to the communities in which we operate.

Ready to make a difference? Apply now!