
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
🐊 Florida, South Carolina – 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 identifying potential sites • Perform study start-up activities, including collecting regulatory documents and supporting contract and budget negotiations • Train sites to collect data properly and report potential safety-related events • Manage site activities during study maintenance • Close down research activities at sites after study conclusion • Conduct study initiation visits (SIVs) • Ensure compliance with informed consent requirements, safety-event reporting, and applicable regulatory requirements • Travel regionally as required
• 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 Psychiatry is required • Must reside in the Southeastern United States • Willingness to travel regionally required
• Competitive benefits package depending on location • Professional development support through regular touchpoints and coaching conversations with the Line Manager • Clear career path and development that can lead to Clinical Trial Manager roles • Support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs • Accessible Executive Leadership team • Inclusive and equitable workplace • Transparent compensation and pay equity
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