Senior Clinical Research Associate – CNS/Oncology

🔥 27 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🇬🇧 UK Skilled Worker Visa Sponsor

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

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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

• Lead site qualification, initiation, interim monitoring, management, and close-out activities • Protect patient safety and data quality by reviewing informed consent, safety information, source documentation, CRFs, and protocol compliance • Partner with investigators and site teams to resolve data queries and maintain regulatory, ethical, Trial Master File, and Investigator Site File documentation • Coordinate CRAs as a Lead CRA on global studies and evaluate study milestones and deliverables with Project Management • Mentor less experienced CRAs and site staff through accompanied visits, monitoring report feedback, and study-specific training • Develop monitoring plans, tools, and templates • Coordinate shipment and receipt of study materials • Ensure investigational product receipt, accountability, return, or destruction • Contribute clinical monitoring expertise to study team and investigator meetings, bid defenses, protocols, and CRFs • Manage sites across the study lifecycle from qualification and initiation through ongoing monitoring and close-out

🎯 Requirements

• MD or Pharmacy degree (MSPH, PharmD, PhD, or equivalent) with at least 3 years of CRA experience; or a four-year degree in medical, biological, physical, health, pharmacy, or another related science with at least 5 years of CRA experience; or a two-year college curriculum or equivalent education/training, preferably nursing or life sciences, with at least 7 years of CRA experience • Extensive knowledge of clinical research principles and processes, GCP, SOPs, FDA and/or EU regulations and directives, ICH Guidelines, and applicable local regulatory requirements • Strong therapeutic-area expertise across two to three therapeutic areas • Demonstrated leadership and communication skills, with ability to mentor colleagues, guide site teams, solve problems, manage priorities, and contribute to process improvements • Proficiency with Microsoft Office, IxRS, and EDC systems • Experience in full-service monitoring preferred • Valid current passport and driving licence • Proficiency in spoken and written English • Must reside in the United Kingdom • Approximately 8–10 days per month of travel to investigative sites

🏖️ Benefits

• Collaborative and inclusive environment • Growth and career development opportunities • Opportunity to learn, grow, and shape the future of clinical research

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