
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.
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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.
• Lead the delivery of Phase I-IV clinical trials from study start-up through closeout • Direct cross-functional project teams and coordinate internal stakeholders, clients, vendors, and subcontractors • Develop, maintain, and adapt project plans, timelines, and resource strategies • Manage project budgets and financial performance • Serve as the primary client contact and drive customer satisfaction • Identify project risks, evaluate operational challenges, and implement solutions • Foster collaboration and resolve conflicts across global and multicultural teams • Ensure project deliverables meet quality, timeline, regulatory, and client expectations • Drive continuous improvement initiatives to enhance operational efficiency and project execution quality
• University or college degree, preferably in Life Sciences, or qualification in a related allied health profession; equivalent combinations of education and experience will also be considered • At least 5 years of clinical pharmaceutical industry experience • Proven Oncology clinical project management experience • Alternatively, significant healthcare supervisory and clinical research experience within pharmaceutical or CRO environments • Demonstrated success leading multidisciplinary and cross-functional project teams in a clinical research setting • Strong knowledge of project management principles, including time, quality, cost, resource planning, and risk management • Solid financial acumen, including experience developing and managing project budgets • Thorough understanding of ICH-GCP guidelines and international regulatory requirements for clinical development programs • Experience using project management software • Ability to manage multiple priorities in a fast-paced environment • Proficiency in English, both written and verbal • Fluency in the local office language is also required
• Collaborative and inclusive work environment • Growth and career development opportunities • Opportunity to learn and shape the future of clinical research • Remote work • Domestic and international travel opportunities as needed
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