Senior Statistical Programmer, SAS Programmer

🔥 5 minutes ago

🌐 Poland, Hungary, +2 more countries – Remote

🇵🇱 Poland – Remote 🇭🇺 Hungary – Remote 🇷🇴 Romania – Remote 🇷🇸 Serbia – Remote

💵 zł200k - zł260k / year

⏰ Full Time

🟠 Senior

🖥 Software Engineer

👻 Ghost score 0%

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • 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.

📋 Description

• Create SAS programs generating derived analysis datasets and content for tables, listings, and figures • Perform programming validation for analysis datasets and programming outputs • Provide programming support to project teams • Develop programming strategies, standards, specifications, and programmed analyses • Support electronic submission preparation and review • Review statistical analysis plans, data presentation plans, and data review plans • Assess the impact of planning documents on programming activities • Interact with vendors regarding project standards, programming conventions, specifications, and file transfers • Ensure quality of deliverables by applying standards and complying with regulatory requirements, guidance, SOPs, and work practices • Identify opportunities to improve efficiency and consistency within the team and vendor interactions • Independently lead and/or perform programming assignments with minimal supervision • Support improvement initiatives

🎯 Requirements

• Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences required • Proficiency in SAS • Several years of clinical / statistical programming experience within pharmaceutical clinical development • Demonstrated proficiency in analytical programming • In-depth understanding of clinical data structure, including CDISC standards, and relational databases • Skills using MS Office, XML, and Pinnacle 21 • Ability to handle and process upstream data, including multiple data forms, workflow, eDC, and SDTM • Ability to provide outputs meeting downstream requirements, including ADaM, Data Definition Table, and e-submission • Good understanding of regulatory, industry, and technology standards and requirements • Good knowledge of statistical terminology, clinical tests, medical terminology, and protocol designs • Ability to work in a team environment with clinical team members

🏖️ Benefits

• Long-term job security and prospects • Flexible work arrangement • Fully home based work option • Office access with desk available for employees who live close to the office • Open and friendly work environment • Opportunities to develop long-term careers • Opportunities to develop within the role and tackle further responsibilities • Opportunities to develop skill sets within other related departments • Incentive plans, bonuses, and/or other forms of compensation may be available • Health, welfare, and other employee benefits