Clinical Research Associate – Oncology, Hematology

🔥 16 hours ago

🌐 Czechia, Slovakia – Remote

🇨🇿 Czechia – Remote 🇸🇰 Slovakia – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

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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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• Conduct site qualification, initiation, interim monitoring, site management, and study close-out visits • Provide mentoring and guidance to less experienced CRAs and site staff when needed • Document site visit findings via written reports • Assess, monitor, and train study site staff on protocol adherence • Review study subject safety information and informed consent • Conduct source document verification for compliance, patient safety, and data veracity • Review CRFs using paper or electronic data capture systems and assist sites with data query resolution • Update site-related documentation for filing in the Trial Master File (TMF) • Ensure site compliance with investigational product receipt, accountability, and return or destruction • Conduct accompanied site visits for assessment or training of other CRAs

🎯 Requirements

• Excellent interpersonal, oral, and written communication skills in English • Superior organizational skills with attention to details • Ability to work with little or no supervision • Proficiency in Microsoft Office, CTMS and EDC Systems • 2+ years of experience as a Clinical Research Associate • 4-year university degree or RN/BSN in Nursing • Experience in Oncology and Hematology is required • Willingness to travel required

🏖️ Benefits

• Supportive and team-oriented work environment • Extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs • Diverse and inclusive workplace • Equal employment opportunities