Senior Clinical Research Associate

🔥 18 hours ago

❄️ Minnesota – 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 • Coordinate study start-up activities, including regulatory documentation and contract and budget processes • Conduct PSSVs, SIVs, IMVs, and COVs • 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 • Travel to investigative sites and collaborate with sites, sponsors, and global study teams

🎯 Requirements

• Bachelor's Degree or a Nursing Degree • 5+ years as a regional, traveling Clinical Research Associate • 2 years of required experience monitoring Oncology clinical trials • Requires travel within the specified region; 8–10 days of service monthly • Experience in full-service monitoring preferred • Strong knowledge of clinical trial processes, site management, and regulatory requirements • Candidates must reside within the Midwest territory • Ability to travel to investigative sites approximately 8–10 days per month

🏖️ Benefits

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

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