Senior Clinical Research Associate – CNS

🔥 1 hour ago

🚗 Michigan, Minnesota – Remote

🚗 Michigan – Remote ❄️ Minnesota – Remote

💵 $97k - $193k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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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 clinical research activities at investigative sites participating in Worldwide clinical studies • Identify and assess potential research sites to support successful study execution • Coordinate study start-up activities, including collection of regulatory documentation and support of contract and budget processes • Conduct Pre-Site Selection Visits, Study Initiation Visits, Interim Monitoring Visits, and Closeout Visits • Train site personnel on protocol requirements, data collection processes, and safety reporting expectations • Monitor site performance and provide ongoing support throughout study maintenance activities • Ensure compliance with informed consent requirements, safety reporting obligations, and applicable regulatory standards • Partner with sites and study teams to drive data quality, participant safety, and overall study success • Support site closeout activities and ensure study requirements are completed at the conclusion of the trial

🎯 Requirements

• Bachelor's Degree or a Nursing Degree • 5+ years as a regional, traveling Clinical Research Associate • Required experience monitoring CNS clinical trials • Requires travel within the specified region; 8–10 DOS monthly • Experience in full-service monitoring preferred • Strong knowledge of clinical trial processes, site management, and regulatory requirement