Senior Clinical Research Associate – Oncology

🕒 May 22

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Logo of Worldwide Clinical Trials

Worldwide Clinical Trials

1001 - 5000 employees

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

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

• Responsible for site qualification, initiation, interim monitoring, site management and study close-out visits for studies in accordance with Good Clinical Practices (GCPs) and applicable regulations and SOPs. • Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. • Conduct study initiation visits (SIVs). • Manage the research activities at sites participating in Worldwide’s clinical research projects.

🎯 Requirements

• 5+ years of experience as a Clinical Research Associate • 4-year university degree OR Nursing Degree • Experience in Oncology is required • Candidates must reside on the East Coast, United States • Willingness to travel regionally required

🏖️ Benefits

• Health insurance • Flexible working arrangements • Professional development opportunities • Paid time off

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