Senior Clinical Research Associate (Oncology) - UK
Overview
We are seeking an experienced Senior Clinical Research Associate (SCRA) to support the monitoring and delivery of Phase I-III oncology clinical trials across the UK. This role is ideal for a proactive, highly organized CRA with strong oncology experience who thrives in a fast-paced, international research environment.
You will be responsible for overseeing multiple clinical trial sites, ensuring compliance with regulatory requirements, and maintaining high standards of data quality and patient safety.
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Key Responsibilities
* Conduct on-site and remote monitoring visits for Phase I-III oncology clinical trials
* Oversee site performance, data quality, and protocol compliance
* Apply and assess RECIST criteria confidently within oncology studies
* Ensure compliance with ICH-GCP, regulatory requirements, and study protocols
* Identify, anticipate, and escalate study-related issues, developing effective solutions
* Build strong relationships with investigators, site staff, and internal stakeholders
* Prepare accurate and timely monitoring reports and documentation
* Support early-phase oncology studies where required
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Education & Experience
* Bachelor's degree (BSc, BA, RN, or equivalent) in a biological or science-related field, or equivalent experience
* Minimum of 5 years' experience as a Clinical Research Associate
* Proven track record of on-site monitoring in oncology trials
* Experience monitoring Phase I-III oncology studies (early phase experience required)
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Skills & Competencies
* Strong working knowledge of ICH-GCP and regulatory requirements
* Excellent multitasking, execution, and problem-solving skills
* High level of organizational ability, efficiency, and attention to detail
* Outstanding interpersonal, communication, and presentation skills
* Ability to work collaboratively within a team environment
* Strong written and verbal communication skills
* Proficient in Microsoft Outlook, Word, and Excel
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Additional Requirements
* Fluent in English and Spanish
* Willingness and ability to travel domestically and internationally as required
o Travel expectation: approximately 6-7 days per month
* Ability to commute within 1 hour of a major airport or railway station
* Valid driver's license and passport preferred
* Successful completion of background clearance checks
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Study & Site Details
* Number of studies: approximately 1-3
* Number of sites: 4-7
* Site locations include: Manchester, London, Glasgow, Liverpool, Sheffield, and Cardiff
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Candidate Profile (Essential Criteria)
* At least 5 years of oncology CRA on-site monitoring experience
* Confident application of RECIST criteria
* Experience monitoring Phase I-III oncology trials
* Based in the UK with strong travel flexibility