
1001 - 5000 employees
🧬 Biotechnology
đź’Š 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.
🔥 24 minutes ago
🌲 North Carolina – Remote
đź’µ $54.5k - $107.5k / year
⏰ Full Time
🟡 Mid-level
đźź Senior
đź‘” Manager
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1001 - 5000 employees
🧬 Biotechnology
đź’Š 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.
• Collaborate with Business Development, Therapeutic Leaders, Operations, Finance and Legal departments to draft and finalize contracts/change orders and contract termination documents with sponsors. • Lead and participate in conference calls to negotiate terms of an agreement, including the study budget, with the sponsor. • Ensure the scope of work is defined correctly and reflected in the study budget. • Ensure any changes are integrated into the main study contract efficiently and accurately. • Revise final proposal budget to reflect agreed upon specifications to include minor changes to the budget including updates to sponsor bid grids, if used, to reflect the revised budget. • Develop and/or modify service description text in addition to original proposal text, which collectively becomes the core contract/exhibit.
• Bachelor's degree or equivalent work experience • Two to three years of direct experience with CRO or pharmaceutical data; sourcing, integration, analysis, and reporting • Advanced Proficiency in MS Office (Word, Excel, PowerPoint)
• Competitive benefits package depending on location • Transparent compensation
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