Clinical Research Associate – Home-based

🔥 29 minutes ago

🇨🇿 Czechia – Remote

⏳ Contract/Temporary

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 12%

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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Alcedis - a HUMA company

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 1992

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Alcedis - a HUMA company is a global contract research organization (CRO) that organizes and executes data-driven clinical studies and advances digital clinical research through proprietary technologies. It combines end-to-end clinical services — including project management, data management, monitoring, regulatory affairs, biostatistics, medical writing and pharmacovigilance — with software platforms (adaptive eCRFs, mobile apps, integrations) and AI/data-science capabilities to support biotech and pharmaceutical development from early-phase trials through regulatory approval and real-world evidence. Alcedis emphasizes technology-first, SaaS-style platforms to improve efficiency, data quality and patient-centric outcomes.

📋 Description

• Support the Clinical Operations team in an international non-interventional study • Independently manage approximately 10 study sites throughout the Czech Republic • Act as the local point of contact for the international project team • Conduct site qualification and feasibility activities • Perform site management, initiation, monitoring and close-out visits on-site and remotely • Prepare visit reports • Conduct source data verification • Support audits and inspections at study sites • Manage data queries in collaboration with data management and project management • Provide EDC training for site staff • Prepare study submissions and notifications to Ethics Committees and, where required, local authorities • Interact with local regulatory authorities • Manage site contracts in the Czech Republic • Travel regularly to study sites across the Czech Republic

🎯 Requirements

• 5 or more years of experience as a CRA in GCP-compliant clinical research in the industry (e.g. CRO, pharma or biotech) • Experience working on multinational non-interventional studies • Confidence working with English-language study documentation, including protocols, monitoring plans, manuals and eCRF guidelines • Strong knowledge of local regulatory requirements in the Czech Republic • Hands-on experience with submissions, interactions with local authorities and site contract management • Fluent Czech and English, written and spoken • Live in the Czech Republic • Willingness to travel regularly to sites nationwide • Independent contractor status (IČO)

🏖️ Benefits

• A fixed-term freelance engagement (independent contractor, IČO) of approx. 60 hours per month for around 10 months • A varied role with a high degree of responsibility and independence • Collaboration with an experienced, international project team • Flexible, home-based working