Worldwide Clinical Trials
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.
In-House Clinical Research Associate
🔥 10 minutes ago
🗣️🇩🇪 German Required
🗣️🇵🇱 Polish Required
🗣️🇮🇹 Italian Required
📊 Check your resume score for this job
Improve your chances of getting an interview by checking your resume score before you apply.
Worldwide Clinical Trials
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
• Ensure quality of data submitted from study sites and assure timely submission of data • 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
🎯 Requirements
• 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 or other experience deemed relevant • Proficiency in English and at least one of the following languages: German, Polish or Italian.
🏖️ Benefits
• Health insurance • Remote work options • Paid time off • Professional development opportunities • Inclusive workplace culture
Apply NowSimilar Jobs
🕒 July 14
Clinical Research Associate designing and analyzing clinical trials for ICON. Conducting site monitoring and ensuring data integrity and patient safety.
🕒 July 3
Clinical Research Associate II monitoring clinical studies for Precision for Medicine in Spain. Ensuring compliance with regulatory standards and managing study progress at investigative sites.
🇪🇸 Spain – Remote
💰 $75M Private Equity Round on 2015-12
⏰ Full Time
🟢 Junior
🟡 Mid-level
🔬 Research Analyst
🕒 July 3
Clinical Research Associate II monitoring clinical studies for Precision Medicine Group based in Spain. Ensuring compliance, coordinating activities, and managing clinical trial progress with travel commitments.
🕒 June 26
Clinical Research Associate performing remote monitoring and site management for clinical trials with global pharmaceutical companies. Ensuring compliance with protocols and regulations while providing support to investigative sites.
