Senior Statistical Programmer

September 30

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Parexel

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Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions

10,000+

💰 Venture Round on 1990-01

Description

• Ability to fill Statistical Programming Lead role on projects. • Ensure quality control (QC) is performed on all process and technical activities. • Provide relevant training and mentorship to staff and project teams. • Maintain and expand local and international regulatory knowledge within the clinical industry. • Proactively participate in and/or lead process/quality improvement initiatives. • Represent Parexel at sponsor marketing and technical meetings.

Requirements

• Excellent analytical skills. • Proficiency in SAS. • Extensive knowledge and understanding of the programming and reporting process. • Knowledge of SOPs/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. • Strong project management skills. • Strong organizational skills, ability to manage competing priorities, and flexibility to change. • Attention to detail. • Ability to successfully lead 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. • Business/operational skills that include customer focus, commitment to quality management, and problem solving. • Demonstrate commitment to refine quality processes. • Good presentation skills. • Good business awareness/business development skills (including financial awareness).