Senior Clinical Research Associate – Oncology

🔥 0 minutes ago

🗽 New York, Massachusetts – Remote

🗽 New York – Remote 🍂 Massachusetts – 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 PSSVs, SIVs, IMVs, and COVs • Train site personnel on protocols, data collection, and safety reporting • Monitor site performance and provide ongoing study maintenance support • 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 activities 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 Oncology clinical trials • Requires travel within the specified region; 8–10 DOS monthly, with some visits remote • Experience in full-service monitoring preferred • Strong knowledge of clinical trial processes, site management, and regulatory requirements • Candidates must reside within the Northeastern United States • Ability to travel to investigative sites approximately 8–10 days per month

🏖️ Benefits

• Competitive benefits package depending on location • Inclusive and equitable workplace • Growth and learning opportunities • Collaborative and inclusive environment

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