Statistical Programmer Lisboa

Statistical Programmer
Lisboa
Lisboa, Lisboa, Portugal

At Capgemini Engineering, the world leader in engineering services, we bring together a global team of engineers, scientists, and architects to help the world’s most innovative companies unleash their potential. From autonomous cars to
- saving robots, our digital and software technology experts think outside the box as they provide unique R&D and engineering services across all industries. Join us for a career full of opportunities. Where you can make a difference. Where no two days are the same.

Your Role

Programs all tables, listings and graphs necessary for an assigned clinical study report (CSR);

Programs customized data displays, (including data listings, summary tables and routine graphics) in accordance with the approved statistical analysis plan (SAP) and shell displays for clinical research studies;

Writes code using Base SAS programs, SAS procedures, or standardized macros;

Analyzes protocol, SAP, existing shells/templates as needed to understand structure and content of data;

Performs data checks as needed, to ensure integrity and correctness of data displays;

Prepares documentation for programs;

Prepares documentation describing all datasets and variables within, including derived variables, and the project as a whole;

Creates SAS datasets of clinical data from clinical databases;

Creates status and efficacy datasets;

Creates
- specific macros and formats;

Loads client data from other platforms and other software packages;

Prepares data to be sent to clients and as needed for other external transfers and data imports.

Your Profile

Communicate effectively in English, in both writing and verbal.

Learn quickly and pay attention to details.

Manage multiple tasks/projects, effectively prioritize and execute tasks, and make quality and on time deliveries.

Work collaboratively, effectively, and productively in diverse organizational structures, and in interaction with dynamic clients.

Work independently, takes ownership and strives for quality and efficiency.

Work positively in a continually changing environment.

Solid/Advanced SAS skills and understanding of the concept of standardization in data, programming, and statistical reporting of trial results and its implication to drug development.

Must have:

At least 5 years experience ADa
M/TLF;

Work in detail (e. g during programming, try to identify any issues on spec/sap/shell instead of just following; identify inconsistency between spec/sap/TLF. );

Good at SAS syntax and SAS macro;

Has experience on safety ADa
M/TLF production side instead of validation side;

Has some knowledge on ADa
M CDISC guidline

What You'll Love About Working Here

• Join a multicultural and inclusive team environment.
• Enjoy a supportive atmosphere promoting
  - life balance.
• Hybrid work.
• Your career growth is central to our mission. Our array of career growth programs and diverse professionals are crafted to support you in exploring a world of opportunities.
• Access valuable training and certifications in
  - edge technologies.
• Engage in exciting national and international projects.
• Health and life insurance.
• Referral program with bonuses for talent recommendations.
• Great office locations.

About Capgemini

Choosing Capgemini means choosing a company where you will be empowered to shape your career in the way you’d like, where you’ll be supported and inspired by a collaborative community of colleagues around the world, and where you’ll be able to reimagine what’s possible. Join us and help the world’s leading organizations unlock the value of technology and build a more sustainable, more inclusive world.