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.
Associate Director, Contract Management
Job not on LinkedIn
🔥 7 minutes ago
🌲 North Carolina – Remote
💵 $118.5k - $234.5k / year
⏰ Full Time
🟠 Senior
🛒 Procurement
🦅 H1B Visa Sponsor
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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
• Advise on legal contractual input and strategy • Ensure submissions are in line with BD requirements and sponsor needs/requests • Manage the overall process and activities for ensuring execution of MSAs, contracts and change orders • Collaborate with BD, therapeutic leaders, Operations and Finance
🎯 Requirements
• Minimum of 10 years of direct experience with CRO or pharmaceutical data • Proficiency in all MS-Office applications including Microsoft Word, PowerPoint, and Excel • In-depth knowledge of the CRO/pharmaceutical industry and sales support activities • Ability to advise and interact with all levels of staff • Strong understanding of study design, project management, and operational requirements
🏖️ Benefits
• Competitive benefits package depending on location • Pay equity and transparency • Compliance with all applicable labor laws • Discussion of salary information during the interview process
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