Associate RTSM Specialist – UK/US

🔥 0 minutes ago

🌐 United Kingdom, United States – Remote

🇬🇧 United Kingdom – Remote 🇺🇸 United States – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🚫👨‍🎓 No degree required

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

👻 Ghost score 10%

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

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.

📋 Description

• Manage RTSM study amendments, ensuring deliverables are completed on time, within scope, and according to quality standards • Coordinate and communicate RTSM project activities with sponsors, study teams, and internal stakeholders • Serve as the primary escalation point for RTSM maintenance activities and drive issue resolution through completion • Monitor study randomisation processes to ensure accurate execution and study integrity • Create and execute User Acceptance Testing (UAT) plans and facilitate sponsor participation • Review, prepare, and approve study support materials, helpdesk documentation, and system-related deliverables • Perform financial reviews and support budget management activities related to change orders • Conduct quality control checks, process study schedules and inventory files, and support ongoing operational activities

🎯 Requirements

• Degree in a relevant discipline or equivalent combination of education and professional experience • Minimum 1 year of RTSM experience • At least 2 years of experience within a CRO or pharmaceutical environment • Experience working within a Contract Research Organisation (CRO) or pharmaceutical setting • Knowledge of RTSM study design, randomisation methodologies, and just-in-time drug supply processes • Understanding of clinical trial conduct, blinding practices, patient safety requirements, data integrity principles, and applicable regulations • Demonstrated ability to manage and support delivery of RTSM solutions used in clinical trials • Strong client-facing, communication, and stakeholder management skills • Proficiency in English with strong written and verbal communication skills • Excellent attention to detail and ability to manage multiple priorities in a fast-paced environment

🏖️ Benefits

• Collaborative and inclusive work environment • Growth and learning opportunities • Opportunity to take ownership of live RTSM projects • Opportunity to collaborate across functions and with global teams • Meaningful work contributing to life-changing clinical research