
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.
🕒 August 9
🏄 California, Nevada – 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, safety-event reporting, and applicable regulatory requirements while managing sites 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 CNS/Neurology is required • Candidates must reside in the Central United States • Willingness to travel regionally required
• Competitive benefits package depending on location • Transparent compensation and pay equity • Professional development support, clear career path, and coaching conversations • Support through regulatory submissions, TMF management, and in-house CRAs • Supportive and team-oriented environment • Accessible Executive Leadership team • Inclusive and equitable workplace
Apply Now🕒 August 8
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