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.
Clinical Research Associate II – Psychiatry
🕒 June 22
🌲 North Carolina – Remote
💵 $79.5k - $158.5k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
🦅 H1B Visa Sponsor
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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
• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects • Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort • Perform various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets • Conduct study initiation visits (SIVs)
🎯 Requirements
• 2 - 5 years of experience as a regional, traveling Clinical Research Associate • 4-year university degree OR Nursing Degree • Experience in Psychiatric monitoring is required • Willingness to travel regionally required
🏖️ Benefits
• Competitive benefits package depending on location • Ensuring pay equity and transparency
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