Senior Statistical Programmer – FSP

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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

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

• Provide technical expertise for the conduct of clinical trials. • Act as an internal subject matter expert in specific areas, providing technical support and expert advice. • 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 the electronic submission preparation and review. • Review key planning documents to ensure alignment with objectives and clarity of programming assumptions. • Interact with vendors regarding project standards and programming specifications. • Provide leadership for ensuring quality of deliverables by applying standards and complying with regulations. • Identify opportunities for increased efficiency and consistency.

🎯 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. • Skills in using software tools such as MS office, XML, Pinnacle 21. • Ability in handling and processing upstream and downstream data forms and outputs. • Good understanding of regulatory, industry, and technology standards and requirements. • Knowledge of statistical terminology, clinical tests, medical terminology, and protocol designs. • Ability to work in a team environment with clinical team members.

🏖️ Benefits

• Competitive financial packages • Training and development • Fully flexible work arrangement • Supportive and dynamic team environment