Senior Associate, Bioinformatics Scientist

Job not on LinkedIn

🔥 0 minutes ago

🌐 United Kingdom, Germany, +6 more countries – Remote

🇬🇧 United Kingdom – Remote 🇩🇪 Germany – Remote 🇫🇷 France – Remote 🇪🇸 Spain – Remote 🇷🇴 Romania – Remote 🇷🇸 Serbia – Remote 🇱🇹 Lithuania – Remote 🇵🇱 Poland – Remote

⏰ Full Time

🟠 Senior

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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

• Support ad hoc requests and updates to analyses and outputs, including figures with different splits/subsets, labels, groupings, color palettes, and formatting while preserving underlying statistical results • Run and optimize automated processing pipelines • Perform routine QC on outputs and document run parameters, versions, and deviations • Execute QC checks on data and result deliverables, generate QC summaries, and route issues for resolution • Refresh RMarkdown/Quarto or Shiny data viewers using approved templates for single-study and cross-study exploration • Package and publish outputs in the agreed team format • Contribute to cross-study data collation, standardization, and ingestion, including variable mapping, identifier harmonization, join validation, and ETL checks • Generate balanced randomization layouts using the approved algorithm • Validate balance metrics and coordinate downstream sample list submission steps • Maintain a reusable library of Claude Code prompts, snippets, and skills • Define standards for style, testing, and documentation • Provide light enablement for consistent AI-assisted workflows • Work within existing analysis plans and technical frameworks, escalating matters requiring advanced scientific interpretation and presentation

🎯 Requirements

• Experience in open-source programming such as R, R Shiny, and bash • Experience using version control tools (git) • Experience using Claude Code and other AI tools • Familiarity with basic statistical modeling fundamentals (linear/logistic models, survival concepts, multiple testing awareness) • Detail oriented with a QC mindset and validation • Good communication and collaboration skills • Comfortable with quick paced environment • BS in Bioinformatics, Computer Science, Computational Biology, Life Sciences, or related discipline • 2+ years of programming experience • Preferably experience in life sciences processing molecular data and/or clinical trial data in the biotechnology, pharmaceutical, or health-related industry • Must live and have the right to work in one of the listed EMEA countries • Required programs: R, Python, R Shiny, bash