Statistical Programmer II – FSP

🔥 19 hours ago

🌐 Poland, Romania, +2 more countries – Remote

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

⏰ Full Time

🟡 Mid-level

🟠 Senior

🖥 Software Engineer

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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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

• Provide technical expertise for the conduct of clinical trials • Support programming activities related to the analysis and reporting of clinical study data with minimal supervision • Potentially fill the Statistical Programming Lead role, or part of it, on small, non-complex projects • Deliver high-quality service using client systems and following client processes • Work closely with client teams and Parexel colleagues in a global environment • Produce derived datasets, including SDTM and ADaM, tables, figures, and data listings of any complexity • Quality-control low-medium complexity derived datasets, tables, figures, and data listings • Develop and QC derived dataset specifications and other process-supporting documents • Maintain complete traceability and regulatory compliance • Participate in and contribute to programming community knowledge-sharing sessions

🎯 Requirements

• Bachelor’s degree in statistics, biostatistics, mathematics, computer science or life sciences • Minimum 3 years of SAS programming experience in clinical research • Proficiency in SAS Base, SAS/STAT, SAS/GRAPH, and SAS macros • Strong understanding of CDISC standards • Knowledge of statistical terminology, clinical tests, and protocol designs • Excellent attention to detail with a focus on quality • Strong written and verbal English communication skills

🏖️ Benefits

• Fully flexible work arrangement; you can be fully home based • Open and friendly work environment • Opportunities to develop long-term careers • Opportunity to develop within the role and take on further responsibilities • Opportunity to develop skill sets within other related departments • Long-term job security and prospects