Medical or Life Sciences Data Curator

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🔥 36 minutes ago

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Expedock

WebsiteLinkedInAll Job Openings

51 - 200 employees

Expedock is the AI-powered automation service behind some of the leading players in the 7 trillion USD global supply chain. We are on a mission to build the powerful data infrastructure that will drive unprecedented efficiency and profitability to all players in the industry.

📋 Description

• Review source materials such as Clinical trial registry updates, Pharma / biotech press releases, Medical or scientific publications, Conference abstracts, Regulatory updates, Patent updates, Company pipeline or asset updates, Medical affairs or drug safety updates, Product, indication, or development milestone announcements. • Determine whether the item should be included in a weekly monitoring report. • Apply clear inclusion / exclusion criteria. • Identify the relevant company, product, asset, indication, mechanism of action, study, or update. • Summarize the key information in concise, source-grounded language. • Verify claims against the original source. • Flag ambiguity, missing information, or uncertain relevance. • Maintain structured data in a consistent format. • Perform quality checks for accuracy, completeness, and clarity.

🎯 Requirements

• Strong attention to detail • Ability to read and understand medical / scientific materials • Clear written English • Ability to summarize complex information concisely • Comfort working with structured templates or spreadsheets • Ability to follow detailed rules and criteria • Strong source-verification habits • Ability to distinguish material updates from non-relevant information • Comfort asking clarifying questions when source information is incomplete • Reliability and consistency in repeated review tasks • Experience with ClinicalTrials.gov (preferred) • Experience with PubMed or scientific publications (preferred) • Experience in pharmacovigilance or regulatory affairs (preferred) • Experience in medical writing or clinical document QC (preferred) • Experience with clinical trial management systems or clinical data systems (preferred) • Familiarity with pharma / biotech pipelines (preferred) • Familiarity with oncology, immunology, rare disease, or other therapeutic areas (preferred) • Experience in data annotation, data curation, or human evaluation work (preferred) • Experience using AI tools for research support, while still verifying outputs against primary sources (preferred).

🏖️ Benefits

• Supportive Remote Environment: Work from home alongside a collaborative team that values growth and mutual success. • Seamless Onboarding & Training: Get up to speed quickly with a structured program and client specific training designed to make you a subject matter expert in your assigned workflows.