Senior Clinical Research Associate – CNS/Oncology

🔥 21 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 in accordance with protocols, GCP, applicable regulations, and SOPs • 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 and ethical documentation • Support the Investigator Site File and provide required documentation for the Trial Master File • Coordinate CRAs as a Lead CRA on global studies, working with Project Management to evaluate study milestones and deliverables • Mentor less experienced CRAs and site staff, including conducting accompanied visits, providing monitoring report feedback, and delivering study-specific training • Develop monitoring plans, tools, and templates and coordinate shipment and receipt of study materials • Ensure appropriate investigational product receipt, accountability, return, or destruction at assigned sites • Contribute clinical monitoring expertise to study team and investigator meetings, bid defenses, and development of protocols and CRFs • Travel to investigative sites approximately 8–10 days per month

🎯 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 the ability to mentor colleagues, guide site teams, solve problems, manage priorities, and contribute to monitoring and site-management process improvements • Proficiency with Microsoft Office, IxRS, and EDC systems • Experience in full-service monitoring preferred • A valid current passport and driving licence • Proficiency in spoken and written English • Must reside in the United Kingdom

🏖️ Benefits

• Collaborative and inclusive environment • Growth and career development opportunities • Opportunity to learn and grow • Meaningful work improving patient lives through clinical research