Senior Clinical Research Associate - Oncology, CNS, Rare Disease - UK - Remote
Job Overview
Location
Virtual United Kingdom
Job Type
Full-time
Category
Marketing
Date Posted
June 3, 2026
Full Job Description
đź“‹ Description
- • Responsible for conducting site qualification, initiation, interim monitoring, site management, and study close-out visits for oncology, CNS, and rare disease clinical trials.
- • Provide mentoring and guidance to less experienced Clinical Research Associates and site staff to ensure consistent protocol adherence and operational excellence.
- • Document all site visit findings through detailed, accurate written reports compliant with regulatory and sponsor requirements.
- • Assess, monitor, and train site personnel on protocol-specific procedures, GCP standards, and regulatory compliance.
- • Review study subject safety data and informed consent documents to ensure patient protection and regulatory integrity.
- • Perform source document verification to validate the accuracy, completeness, and veracity of clinical data collected at investigational sites.
- • Review Case Report Forms (CRFs) using electronic data capture (EDC) systems and assist sites in resolving data queries promptly.
- • Maintain and update site-related documentation for inclusion in the Trial Master File (TMF) to ensure audit readiness.
- • Ensure strict compliance with investigational product (IP) receipt, accountability, storage, return, and destruction procedures as per protocol and regulatory guidelines.
- • Conduct accompanied site visits to assess or train other CRAs as requested, supporting team development and quality assurance.
- • Work independently with minimal supervision while maintaining high standards of accuracy, timeliness, and regulatory compliance.
- • Utilize Microsoft Office, Clinical Trial Management Systems (CTMS), and EDC platforms to manage trial documentation and data workflows.
- • Travel to investigational sites across the United Kingdom as required to perform on-site monitoring activities.
- • Apply specialized knowledge of oncology, central nervous system (CNS), and rare disease clinical trial protocols to ensure high-quality trial execution.
- • Demonstrate superior organizational skills and meticulous attention to detail in managing multiple trial sites and documentation requirements.
- • Maintain clear, professional communication with site staff, sponsors, and internal teams through written and verbal interactions in English.
🎯 Requirements
- • 5+ years of experience as a Clinical Research Associate
- • 4-year university degree or RN/BSN in Nursing
- • Must have direct experience in oncology, CNS, and rare disease clinical trials
- • Willingness to travel within the United Kingdom
- • Proficiency in Microsoft Office, CTMS, and EDC systems
- • Excellent interpersonal, oral, and written communication skills in English
🏖️ Benefits
- • Opportunity to work with a global CRO committed to advancing breakthrough scientific research
- • Supportive, collaborative, and inclusive team environment that values diversity and employee well-being
- • Role with meaningful impact on patient outcomes in oncology, CNS, and rare disease therapies
- • Position offering autonomy and professional growth within a values-driven culture
Skills & Technologies
About Worldwide Holdings Corporation
Worldwide Holdings Corporation is a diversified global enterprise engaged in the development, manufacturing, and marketing of a wide range of products and services. The company operates across various sectors, including technology, consumer goods, and industrial solutions, with a strong focus on innovation and sustainability. Worldwide Holdings Corporation is committed to delivering high-quality products and exceptional customer service, aiming to foster long-term relationships with its clients and stakeholders. The company's strategic vision involves expanding its global reach, investing in research and development, and adapting to evolving market demands to maintain a competitive edge in the international marketplace. Their mission is to create value through responsible business practices and a dedication to excellence.
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