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Statistics Opportunities at Parexel

By being hired into one of our Statistics Programming jobs at Parexel International, you’ll be a key member of the Parexel International team. Professionals in Statistics Programming careers come from a variety of backgrounds, bringing an assortment of knowledge and skills to every area of our business. A job in Statistics Programming at Parexel International may be waiting for you!

Statistical Programmer I/II

Job ID 54424BR Wavre, Wallonia, Belgium
The Statistical Programmer II provides technical expertise for the conduct of clinical trials, and works with minimal supervision to support various programming activities related to the analysis and reporting of clinical study data. In addition, the Statistical Programmer II may fill the Statistical Programming Lead role (or part of that role) on small, non-complex projects. Assist in the coordination of project start-up activities, creation of global programs, tracking spreadsheets, and other required documentation. Deliver best value and high quality service. • Check own work in an ongoing way to ensure first-time quality. • Use efficient programming techniques to produce derived datasets (e.g. SDTM, ADaM), tables, figures, and data listings of any complexity and QC low-medium complexity derived datasets, tables, figures, and data listings. • Assist in the production/QC of derived dataset specifications and other process supporting documents and submission documentation. Maintain and expand local and international regulatory knowledge within the clinical industry. • Develop knowledge of SAS and processes/procedures within other Parexel functional areas. • Provide relevant training and mentorship to staff and project teams as appropriate. Maintain all supporting documentation for studies in accordance with SOPs/Guidelines to ensure traceability and regulatory compliance. • Ensure compliance with SOPs/Guidelines, ICH-GCP, and any other applicable local and international regulations, and participate in internal/external audits and regulatory inspections as required. • Proactively participate in process/quality improvement initiatives. • Understand regulatory requirements concerning industry technical standards (e.g. CDISC, 21 CFR Part 11, and electronic submissions).

Qualifications

Office or Home Based

*Seeking both Statistical Programmers I/II

  • Proficiency in SAS
  • Knowledge of the programming and reporting process
  • 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 application
  • Demonstrated application of CRS concepts to achieve best practice and promote continuous improvement
  • Demonstrate ability to learn new systems and function in an evolving technical environment
  • Ability to successfully work together with a (“virtual”) team (including international teams as required) as well as independently
  • Demonstrate strong organizational skills, ability to manage competing priorities, and be flexible to change
  • Attention to detail.
  • Excellent analytical skills.
  • Good presentation skills.
  • Tenacity to work in an innovative environment.
  • Ability to negotiate and influence in order to achieve results.
  • Business/Operational skills that include customer focus, commitment to quality management and problem solving.
  • Good business awareness/business development skills (including financial awareness).
  • Ability to create, maintain and define strategies to improve the efficiency of running a clinical trial.
  • Work effectively in a quality-focused environment.
  • Demonstrate commitment to refine quality processes.
  • Effective time management in order to meet daily metrics or team objectives
  • Show commitment to and perform consistently high quality work
Education
  • Educated to degree level in a relevant discipline and/or equivalent work experience
Language Skills
  • Competent in written and oral English.
  • Excellent communication skills.

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