
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.
🕒 July 1
🇬🇧 United Kingdom – Remote
⏰ Full Time
🟡 Mid-level
🟠 Senior
💻 Solutions Engineer
🇬🇧 UK Skilled Worker Visa Sponsor
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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.
• Lead end-to-end delivery of patient and site engagement activities across multiple clinical studies • Coordinate and manage Worldwide vendors globally that provide strategic and operational support for specifically awarded projects • Develop and manage detailed project plans, timelines, budgets, and resource allocations • Monitor project performance, proactively identifying risks and implementing mitigation strategies • Ensuring that recruitment and retention objectives are met within assigned studies • Ensure projects are delivered on time, within scope, and aligned with sponsor and regulatory requirements • Collaborate with team members to review patient recruitment strategies’ appropriateness and implementation for various client proposals. • Recommends solutions and escalate issues to Project Management or Patient and Site Solutions team management as required
• 4-5 years’ experience in clinical research related field • Background in medicine, science or other relevant discipline • Understanding of building budgets as they pertain to vendor services • Ability to communicate and negotiate with vendors for relevant services • Effective communicator, both written and spoken English • Knowledge of the principles of Good Clinical Practice • Minimum Bachelor’s degree or equivalent • Travel approximately 5% for business needs • Ability to work at a fast pace with short timelines.
• Flexible work arrangements • Professional development opportunities
Apply Now🕒 June 30
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