
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.
🔥 0 minutes ago
🌽 Illinois, Minnesota – Remote
💵 $97k - $193k / year
⏰ Full Time
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
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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.
• Manage research activities at sites participating in Worldwide’s clinical research projects • Participate in all stages of clinical studies, including site identification, study start-up, site maintenance, and study closeout • Collect appropriate regulatory documents from sites • Support negotiation of contracts and budgets • Train sites to collect data properly and report potential safety-related events • Conduct study initiation visits (SIVs) • Ensure compliance with informed consent, safety-event reporting, and applicable regulatory requirements • Perform most site management efforts remotely
• Excellent interpersonal, oral, and written communication skills in English • Superior organizational skills with attention to detail • Ability to work with little or no supervision • Proficiency in Microsoft Office, CTMS, and EDC Systems • 5+ years of experience as a Clinical Research Associate • 4-year university degree OR Nursing Degree • Experience in Oncology is required • Candidates must reside on the Midwest or Central Regions • Willingness to travel regionally required
• Competitive benefits package depending on location • Professional development through regular touchpoints and coaching conversations with Line Manager • Clear career path and development that can lead to Clinical Trial Manager roles • Supportive and team-oriented work environment • Regulatory submission, TMF management, and in-house CRA support
Apply Now🔥 2 hours ago
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