
1001 - 5000 employees
🏥 Healthcare
đź’Ľ 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.
đź•’ July 18
🌲 North Carolina – Remote
đź’µ $87.5k - $173.5k / year
⏰ Full Time
đźź Senior
đź§Ş Clinical Research
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1001 - 5000 employees
🏥 Healthcare
đź’Ľ 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.
• Independently manages statistical project support • Provides expert statistical consultancy across the statistics function • Manage the statistics support to one or more projects/sponsor programs of work • Provide expert review of study designs, analysis plans, and reports • Assist sponsors in the design of clinical trials • Liaise with internal departments, sponsors, and other third parties regarding statistical issues • Prepare final reports, including the production of tables, listings, figures, and report writing • Develop, test, and run SAS programs for statistical analysis and reporting • Ensure the maintenance of documentation, including descriptions of programs and validation • Make statistical contributions to manuscripts for publication and presentation • Assist the Director of Biostatistics with all other aspects of the job as required • Perform all activities in compliance with Worldwide Clinical Trials and agreed sponsor quality system standards
• Educated to degree level in mathematics, statistics, or another subject with a strong statistical component • Hands-on expert-level project statistician experienced in providing statistical leadership to projects • Design and analysis consultancy skills and knowledge across a broad range of applications • Key competencies in customer focus, delivering on commitments, building strong relationships, communicating and influencing, and embracing innovation and change
• Competitive benefits package depending on location • Pay equity and transparency
Apply Nowđź•’ July 16
Manager for Clinical Data Management in Data Sciences Department responsible for delivering data management services and ensuring quality service with regulatory compliance.
🇺🇸 United States – Remote
đź’µ $99.5k - $166k / year
⏰ Full Time
đźź Senior
đź”´ Lead
đź§Ş Clinical Research
đź•’ July 15
Clinical Research Budgeting Analyst responsible for preparation and maintenance of budgets for clinical trials. Collaborates with internal teams and manages workflow across multiple research programs.
🇺🇸 United States – Remote
đź’µ $37 - $58 / hour
⏰ Full Time
🟡 Mid-level
đźź Senior
đź§Ş Clinical Research
🦅 H1B Visa Sponsor
đź•’ July 15
Oncology Sr. CRA 2 responsible for all aspects of study site monitoring. Ensuring adherence to protocols and maintaining integrity of trial data with considerable travel involved.
🇺🇸 United States – Remote
đź’µ $125k - $140k / year
⏰ Full Time
đźź Senior
đź§Ş Clinical Research
đź•’ July 14
Senior Specialist in Clinical Research Monitoring at Edwards Lifesciences. Conducting field monitoring of clinical trial studies and ensuring adherence to protocols and regulatory compliance.
🇺🇸 United States – Remote
đź’µ $108k - $153k / year
⏰ Full Time
đźź Senior
đź§Ş Clinical Research
🦅 H1B Visa Sponsor
đź•’ July 14
Manager, Clinical Research Monitoring with Edwards improving patient lives through clinical evidence in cardiac innovation. Overseeing clinical trials and ensuring regulatory compliance for groundbreaking medical devices.
🇺🇸 United States – Remote
đź’µ $126k - $178k / year
⏰ Full Time
đźź Senior
đź”´ Lead
đź§Ş Clinical Research
🦅 H1B Visa Sponsor