As a member of PAREXEL’s Statistical Programming group, you will be heavily involved in leading trials to successful completion, working in close collaboration with sponsor teams, and PAREXEL teams in differing locations.
Depending on your career goals, you will be provided the opportunity to be exposed to a variety of different sponsors, products and therapeutic areas, or choose to focus your career on working with a specific sponsor and gaining in depth knowledge of a specific therapeutic area and compound.
You will become a part of a team with an inherent breadth of knowledge and expertise in small, single center Investigator studies to multi-
site, multi-national trials in Phases I to IV of clinical development, as well as observational studies. From initial planning meetings at the study design stage through to implementation and execution, our team of skilled statistical programmers will employ industry-
accepted statistical tools and techniques, as well as innovative consulting, to provide the quality and efficiency of projects.
PAREXEL develops and delivers cost effective, high-quality training programs for those employees that are directly involved with sponsor functional partnerships to ensure that our statistical programmers can quickly step in to make significant contributions to the success of a study.
In addition, you will receive the opportunity to shape your development through quarterly conversations with your manager.
What makes a successful Principal Statistical Programmer at PAREXEL? Check out the top traits we’re looking for and see if you have the right mix.
The Statistical Programmer I works with supervision to support various programming activities related tothe analysis and reporting of clinical study data.
QualificationsExcellent analytical skills.