
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.
🕒 2 days ago
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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.
• Provide management and leadership oversight of teams and projects within Data Management department for study execution and budget management. • Act as the primary point of contact for any study specific escalations (internal or external). • Represent the company at sponsor governance meetings. • Ensure staff are allocated to projects appropriately and according to their abilities/competencies, appropriate oversight, training and mentoring is provided. • Ensure projects within the team are appropriately resourced, operational, or budget risks are discussed and addressed. • Define and monitor objectives for individual team members, ensuring there are opportunities for career and personal development. • Provide support to Business Development staff by participating in preparation of proposals and presentations to sponsors. • Participate as necessary in sponsor audits, regulatory authority inspections and other third party meetings.
• Bachelor’s degree or higher in biomedical sciences, life sciences, computer science or related discipline — or equivalent relevant experience. • Min of 9 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries. • 2-4 years of line management experience. • Expert knowledge of data management best practices & technologies as applied to clinical trials. • Excellent communication and interpersonal skills to collaborate with cross-functional internal and external teams. • Strong project management skills and experience managing data management teams and projects for operational and budget oversight. • Independent analytical and problem solving skills.
• Flexible working hours • Professional development opportunities
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