
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.
🔥 2 hours ago
🗣️🇩🇪 German Required
🗣️🇪🇸 Spanish Required
🗣️🇮🇹 Italian Required
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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.
• Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel • Ensure completeness and compile regulatory documents and ethical submission documentation as appropriate and required (e.g. IRB approval, informed consent, lab certification etc.) • Provide applicable updates for site related documentation for filing in the Trial Master File (TMF) • Perform feasibility studies/site identification activities for potential sites, as requested
• Excellent interpersonal, oral, and written communication skills • Ability to contribute to a team remotely • Strong customer focus, ability to interact professionally with a sponsor contact • Proficiency in Microsoft Office, CTMS, and EDC Systems • Four-year college curriculum with a major concentration in life science preferred but not required, OR Two-year college curriculum or equivalent education/training and one year experience with clinical research (e.g. study coordinator, CTA, etc.) or other experience deemed relevant • Proficiency in English and at least one of the following languages: German, Spanish, or Italian.
• Health insurance • 401(k) matching • Professional development opportunities
Apply Now🔥 5 hours ago
Clinical Research Associate responsible for site management in oncology studies for top pharmaceutical companies. Work from home in Poland with opportunities for mentorship and collaboration.
🇵🇱 Poland – Remote
💵 zł220k - zł240k / year
💰 Venture Round on 1990-01
⏰ Full Time
🟢 Junior
🟡 Mid-level
🔬 Research Analyst
🔥 5 hours ago
Clinical Research Associate managing site activities for oncology studies in Poland. Dedicated to single client and responsible for site management and mentorship of junior CRAs.
🇵🇱 Poland – Remote
💵 zł220k - zł240k / year
💰 Venture Round on 1990-01
⏰ Full Time
🟢 Junior
🟡 Mid-level
🔬 Research Analyst
🕒 July 16
Clinical Research Associate managing oncology studies and supporting a single client at Parexel in Poland. Responsibilities include site management and mentoring junior CRAs with opportunities for travel and remote work.
🇵🇱 Poland – Remote
💵 zł220k - zł240k / year
💰 Venture Round on 1990-01
⏰ Full Time
🟢 Junior
🟡 Mid-level
🔬 Research Analyst
🕒 July 10
Clinical Research Associate designing and analyzing clinical trials to contribute to the advancement of innovative treatments at ICON. Conducting monitoring activities and ensuring compliance in clinical trials.
🕒 July 9
CRA II at ICON designing and analyzing clinical trials to advance healthcare. Collaborating with clinical staff and ensuring protocol compliance during trial processes.