Senior Clinical Research Associate – Oncology

🔥 0 minutes ago

🚗 Michigan, Wisconsin – Remote

🚗 Michigan – Remote 🧀 Wisconsin – Remote

💵 $97k - $193k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🦅 H1B Visa Sponsor

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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 research activities at sites participating in Worldwide’s clinical research projects • Identify potential sites for participation in clinical research • Perform study start-up activities, including collecting regulatory documents from sites • Support negotiation of contracts and budgets • Train sites to collect data properly and report potential safety-related events • Manage site activities during study maintenance • Close down research activities at sites after study completion • Conduct study initiation visits (SIVs) • Perform most site management remotely while ensuring informed-consent, safety-reporting, and regulatory compliance

🎯 Requirements

• Excellent interpersonal, oral, and written communication skills in English • Superior organizational skills with attention to detail • Ability to work with little or no supervision • Proficiency in Microsoft Office, CTMS, and EDC Systems • 5+ years of experience as a Clinical Research Associate • 4-year university degree OR Nursing Degree • Current experience in Oncology is required • CAR-T experience is desired • Fluent in written and verbal English required • Prefer candidates residing in the Midwest • Willingness to travel regionally required

🏖️ Benefits

• Extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs • Regular touchpoints and coaching conversations with Line Manager • Clear career path and professional development leading to Clinical Trial Manager roles • Accessible Executive Leadership team • Competitive benefits package depending on location