
10,000+ employees
Founded 1983
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Venture Round on 1990-01
Consulting âą Healthcare âą Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
đ„ 3 hours ago
đżđŠ South Africa â Remote
â° Full Time
âȘïž Entry-level
đ„ Software Engineer
đ» Ghost score 10%
Improve your chances of getting an interview by checking your resume score before you apply.

10,000+ employees
Founded 1983
đŒ Consulting
đ„ Healthcare
đŠ Logistics
đ° Venture Round on 1990-01
Consulting âą Healthcare âą Logistics
Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.
âą Perform statistical programming for assigned projects âą Deliver high-value, high-quality service âą Check own work continuously to ensure first-time quality âą Use efficient programming techniques to produce low- to medium-complexity derived datasets, including SDTM and ADaM âą Produce tables, figures, and data listings âą Maintain and expand local and international regulatory knowledge within the clinical industry âą Develop knowledge of SAS and processes/procedures within other Parexel functional areas âą Maintain supporting study documentation according to SOPs/Guidelines for traceability and regulatory compliance âą Ensure compliance with SOPs/Guidelines, ICH-GCP, 21 CFR Part 11, and other applicable regulations âą Participate in internal/external audits and regulatory inspections as required
âą Excellent analytical skills âą Knowledge and understanding of the programming and reporting process âą Knowledge of SOPs/Guidelines, ICH-GCP, and applicable local and international regulations such as 21 CFR Part 11 âą Ability to learn new systems and function in an evolving technical environment âą Attention to detail âą Ability to successfully work as part of a global team âą Ability to work effectively in a quality-focused environment âą Effective time management to meet daily metrics or team objectives âą Commitment to consistently high-quality work âą Competent written and oral English âą Good communication skills âą Educated to degree level in a relevant discipline and/or equivalent work experience âą Equivalent work experience may substitute for the degree-level education requirement
âą No benefits, perks, or compensation extras are specified
Apply Now