Statistical Programmer I (SAS Programmer)

The Statistical Programmer I works with supervision to support various programming activities related to the analysis and reporting of clinical study data.

• 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 low medium complexity derived datasets (e.g. SDTM, ADaM), tables, figures, and data listings.

• Maintain and expand local and international regulatory knowledge within the clinical industry.

• Develop knowledge of SAS and processes/procedures within other PAREXEL functional areas.

• Maintain all supporting documentation for studies in accordance with SOP's/Guidelines to ensure traceability and regulatory compliance.

• Ensure compliance with SOP's/Guidelines, ICH-GCP, and any other applicable local and international regulations, and participate in internal/external audits and regulatory inspections as required.Qualifications• Excellent analytical skills.

• Knowledge and understanding of the programming and reporting process.

• Knowledge of SOP's/Guidelines, ICH-GCP, and any other applicable local and international regulations such as 21 CFR Part 11.

• Ability to learn new systems and function in an evolving technical environment.

• Attention to detail.

• Ability to successfully work as part of a global team.

• 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.

• Competent in written and oral English.

• Good communication skills.

• Educated to degree level in a relevant discipline and/or equivalent work experience.