Senior Clinical Research Associate – CNS/Rare Disease

🔥 0 minutes ago

⛰️ Colorado, Oklahoma – Remote

⛰️ Colorado – Remote 🌪️ Oklahoma – Remote

💵 $97k - $193k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

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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 Trials studies • Identify and assess potential research sites • Coordinate study start-up activities, including regulatory documentation and contract and budget processes • Conduct Pre-Site Selection, Study Initiation, Interim Monitoring, and Closeout Visits • Train site personnel on protocol requirements, data collection, and safety reporting • Monitor site performance and provide ongoing support during study maintenance • Ensure informed consent, safety reporting, and regulatory compliance • Partner with sites and study teams to support data quality, participant safety, and study success • Support site closeout and completion of study requirements

🎯 Requirements

• Bachelor's Degree or a Nursing Degree • 5+ years as a regional, traveling Clinical Research Associate • Required experience monitoring CNS and Rare Disease clinical trials • Must reside within the Central part of the United States territory • Requires travel within the specified region, approximately 8–10 days per month • Experience in full-service monitoring preferred • Strong knowledge of clinical trial processes, site management, and regulatory requirements

🏖️ Benefits

• Competitive benefits package depending on location • Inclusive and equitable workplace • Equal employment opportunities • Professional growth and development opportunities • Collaborative and inclusive work environment • Home-based work arrangement

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