Senior Associate, Biomarker Data 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

📊 Data Scientist

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

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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

• Run, monitor, and maintain existing analysis pipelines, internal R packages, and report templates, including interactive data exploration tools • Contribute via git using branching, pull requests, and code review; coordinate handoffs • Manage end-to-end data flow, including requesting data from BDM, tracking delivery, organizing data on internal servers, and maintaining folder structure and data cut documentation • Prepare and send sample lists to sample management and other departments upon request • Work with scientists to harmonize heterogeneous formats for ongoing ingestion of biomarker data into common data formats • Maintain run logs and validate outputs against expected formats and metrics • Ensure raw and processed outputs are stored according to team conventions • Maintain project and deliverable trackers covering status, owners, due dates, dependencies, and links • Provide concise visibility for stakeholders • 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 for consistent AI-assisted coding workflows

🎯 Requirements

• Must live and have the right to work in one of the following EMEA countries only: United Kingdom, Germany, France, Spain, Romania, Serbia, Lithuania, or Poland • 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 • SQL, database design (PostgreSQL/similar), ETL pipelines • HTML/CSS/JavaScript basics • Familiarity with basic statistical modeling fundamentals (linear/logistic models, survival concepts, multiple testing awareness) • QC mindset and validation • Good communication and collaboration skills • Comfortable with quick paced environment • R/R/Python, R Shiny, bash • BS in Bioinformatics, Computer Science, Computational Biology, Life Sciences, or related discipline • 2+ years of programming experience, preferably in life sciences processing molecular data and/or clinical trial data in the biotechnology, pharmaceutical, or health-related industry