Clinical Research Associate II – Metabolic

🔥 1 hour ago

🌵 Arizona, Texas – Remote

🌵 Arizona – Remote 🤠 Texas – Remote

💵 $79.5k - $158.5k / year

⏰ Full Time

🟡 Mid-level

🧪 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 • Coordinate study start-up activities, including regulatory documentation and 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, 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 drive data quality, participant safety, and study success • Support site closeout and completion of study requirements • Travel to investigative sites approximately 8–10 days per month

🎯 Requirements

• Bachelor's Degree or a Nursing Degree • 3+ years as a regional, traveling Clinical Research Associate • Experience monitoring Cardiometabolic and Hypertension 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 requirements • Candidates must reside within the territory • Ability to support site visits and study activities across the Central / West Coast of the United States

🏖️ Benefits

• Competitive benefits package depending on location • Inclusive and equitable workplace • Equal employment opportunities • Transparent compensation and pay equity

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