
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.
🕒 July 1
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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.
• Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects • Conduct study initiation visits (SIVs) • Ensure compliance with obtaining informed consent • Perform various study start-up activities such as working with sites to collect appropriate regulatory documents
• 5+ years of experience as a Clinical Research Associate • 4-year university degree OR Nursing Degree • Experience in Rare Disease required • Candidates must reside in the East Coast or Central United States • Willingness to travel regionally required
• Competitive benefits package depending on location • Pay equity and transparency • Professional development opportunities
Apply Now🕒 June 30
Contract Specialist managing university-wide contract negotiations and serving as liaison between stakeholders and entities. Drafting and negotiating various research agreements and contracts.
🕒 June 30
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🕒 June 30
Senior Clinical Research Associate at ICON managing Oncology clinical trials to ensure data integrity and subject safety. Responsible for site engagement, compliance, and regulatory inspections with a focus on collaboration.
🕒 June 29
Senior Clinical Research Associate responsible for overseeing clinical trials and ensuring quality compliance. Engaging with investigator sites and managing study implementation in accordance to GCP.
🇺🇸 United States – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟠 Senior
🔬 Research Analyst
🦅 H1B Visa Sponsor
🕒 June 26
Senior Clinical Research Associate managing clinical trials at Novartis. Building site relationships and ensuring compliance with regulatory requirements through remote monitoring and support.
🇺🇸 United States – Remote
💵 $108.5k - $201.5k / year
⏰ Full Time
🟠 Senior
🔬 Research Analyst
🦅 H1B Visa Sponsor
🗣️🇪🇸 Spanish Required