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Company overview:

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.


Deliver best value and high quality service.
 Check own work in an ongoing way to ensure first-time quality.
 Maintain all supporting documentation for studies in accordance with WSOPs/Guidelines to ensure traceability and regulatory compliance.
 Ensure compliance with WSOPs/Guidelines, ICH-GCP and any other applicable local and international regulations and participate in internal/external audits and regulatory inspections as required.
 Use efficient programming techniques to produce low-medium complexity derived datasets, tables, figures and data listings.
 Create, implement and execute import and export programs, in either standard format, client specific format or CDISC compliant format depending on nature of request.
 Develop mapping specification for data exports in accordance with applicable standards.
Experience in SAS.
 Knowledge of the programming and reporting process within the Statistical Programming
 Knowledge of WSOPs/Guidelines/System Life Cycle methodologies, ICH-GCP and any other
applicable local and international regulations such as 21 CFR Part 11 and proven practical
 Demonstrate ability to learn new systems and function in an evolving technical environment.
 Attention to detail.
 Ability to successfully work together with a (“virtual”) team (including international teams as
required) as well as independently.
 Work effectively in a quality-focused environment.
 Effective time management in order to meet daily metrics or team objectives.
 Show commitment to and perform consistently high quality work.

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