Senior Statistical Programmer, FSP

September 30

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Parexel

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Healthcare Insurance • Biotechnology • Pharmaceuticals

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.

10,000+ employees

Founded 1983

⚕️ Healthcare Insurance

🧬 Biotechnology

💊 Pharmaceuticals

💰 Venture Round on 1990-01

📋 Description

• Create SAS programs to generate derived analysis datasets and content for tables, listings, and figures • Perform programming validation to ensure quality of analysis datasets and programming outputs • Provide programming support for project teams, including development of programming strategies, standards, specifications, and programmed analysis • Support electronic submission preparation and review • Review key planning documents (statistical analysis plan, data presentation plan, data review plan) and assess impact on programming activities • Interact with vendors regarding project standards, programming conventions, programming specifications and file transfers • Provide leadership to ensure quality of deliverables and compliance with regulatory requirements, guidance and SOPs • Identify opportunities for increased efficiency and consistency with team and vendors • Independently lead and/or perform programming assignments with minimal supervision • Support improvement initiatives and act as subject matter expert dedicated to a single sponsor

🎯 Requirements

• Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences required • Proficiency in SAS • Minimum of 5 years clinical / statistical programming experience within pharmaceutical clinical development • Demonstrated proficiency in analytical programming • In-depth understanding of clinical data structure (e.g., CDISC standards) and relational database • Demonstrated skills in using software tools and applications, e.g., MS office, XML, Pinnacle 21 • Demonstrated ability in the handling and processing of upstream data, e.g., multiple data forms, workflow, eDC, SDTM • Demonstrated ability in providing outputs to meet downstream requirements, e.g., ADaM, Data Definition Table, e-submission • Good understanding of regulatory, industry, and technology standards and requirements • Good knowledge of statistical terminology, clinical tests, medical terminology, and protocol designs • Demonstrated ability to work in a team environment with clinical team members • Applicants must be authorized to work in the UK; employer cannot sponsor a work visa

🏖️ Benefits

• Fully flexible work arrangement - you can be fully home based • Competitive financial packages • Training and development • Smooth induction and training program • Multinational working environment • Healthy work/life balance • Option to use office desk if local