Senior Clinical Research Associate – CNS, Psychiatry

🔥 1 minute ago

🌲 North Carolina – Remote

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💵 $97k - $193k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🦅 H1B Visa Sponsor

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👻 Ghost score 0%

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Logo of Worldwide Clinical Trials

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

• Manage research activities at investigative sites participating in Worldwide clinical research projects • Support sites throughout the clinical study lifecycle, from identification and start-up through maintenance and closeout • Coordinate study start-up activities, including collecting appropriate regulatory documents and supporting contract and budget negotiations • Conduct study initiation visits and train sites on accurate data collection and safety event reporting • Monitor site activities and help ensure compliance with informed consent, safety reporting, and applicable regulatory requirements • Partner with sites and study teams to address site management needs and support successful study delivery • Travel to investigative sites approximately 8–10 days per month • Collaborate with sites, sponsors, and global study teams

🎯 Requirements

• Bachelor’s degree from a four-year university or a Nursing Degree • 5+ years of experience as a Clinical Research Associate • Experience in Psychiatry • Excellent interpersonal, oral, and written communication skills, including proficiency in English • Strong organizational skills with excellent attention to detail and the ability to work with little or no supervision • Proficiency in Microsoft Office, CTMS, and EDC systems • Residence on the East Coast • Willingness to travel regionally • Experience in full-service monitoring PREFERRED

🏖️ Benefits

• Competitive benefits package depending on location • Regular coaching and development conversations • Clear career path that can lead to Clinical Trial Manager opportunities • Inclusive and equitable workplace • Transparent compensation and pay equity

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