Bioinformatics Scientist

🔥 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

🟡 Mid-level

🟠 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 • Build and refresh RMarkdown/Quarto or Shiny data viewers using approved templates for single-study and cross-study exploration • Package and publish data viewer outputs in the agreed team format • Support cross-study database integration through data collation, standardization, ingestion, variable mapping, identifier harmonization, join validation, and ETL checks • Generate balanced Olink randomization layouts using the team’s approved algorithm • Validate Olink balance metrics and coordinate downstream sample list submission steps • Maintain a reusable library of Claude Code prompts, snippets, and skills for common tasks • Define standards for AI-assisted workflows, including style, testing, and documentation • Provide light enablement to support consistent AI-assisted workflows • Work with minimal supervision within existing analysis plans and technical frameworks • Escalate matters requiring advances in scientific interpretation and presentation

🎯 Requirements

• BS in Bioinformatics, Computer Science, Computational Biology, Life Sciences, or related discipline required • 4+ 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 • Knowledge in cardiovascular, metabolic, immunity, hematology, oncology, renal diseases, neurodegenerative disorders, muscle and metabolism disorders, and/or rare genetic diseases • Experience with open-source programming such as R, R Shiny, and bash • Experience using version control tools such as git • Experience using Claude Code and other AI tools • Familiarity with basic statistical modeling fundamentals, including linear/logistic models, survival concepts, and multiple testing awareness • QC mindset and validation • Good communication and collaboration skills • Comfortable with a quick-paced environment • Required equipment/programs: R/R/Python, R Shiny, bash