Senior Clinical Research Associate – CNS, Psychiatry

🔥 12 hours ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $97k - $193k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🦅 H1B Visa Sponsor

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

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’s clinical research projects • Support sites throughout the full study lifecycle, from site identification and start-up through study maintenance and close-out • Coordinate study start-up activities, including collecting required regulatory documentation and supporting contract and budget negotiations • Conduct Study Initiation Visits (SIVs) and train sites on accurate data collection and safety-event reporting • Manage ongoing site activities, primarily remotely, while maintaining effective communication and oversight • Ensure sites comply with informed consent requirements, safety reporting expectations, and applicable regulatory requirements • Partner with site teams to support high-quality study conduct and successful clinical trial delivery • Collaborate with investigative sites, sponsors, and global study teams • Travel to investigative sites approximately 8-10 days per month

🎯 Requirements

• A four-year university degree or Nursing Degree • 5+ years of experience as a Clinical Research Associate • Experience in Psychiatry required • Experience in full-service monitoring PREFERRED • Excellent interpersonal, organizational, and communication skills, with strong attention to detail • Ability to work effectively with little or no supervision • Proficiency in Microsoft Office, CTMS, and EDC systems • Proficiency in English, including strong oral and written communication skills • Candidates must reside within the Southeast territory • Ability to travel to investigative sites approximately 8-10 days per month

🏖️ Benefits

• Regular coaching conversations • Professional development support • Career path that can lead to Clinical Trial Manager opportunities • Competitive benefits package depending on location • Inclusive and equitable workplace