Senior CRA

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.

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

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)

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

Additional Requirements

• Fluent in English and Spanish

• Willingness and ability to travel domestically and internationally as required

  • 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

Study & Site Details

• Number of studies: approximately 1-3

• Number of sites: 4-7

• Site locations include: Manchester, London, Glasgow, Liverpool, Sheffield, and Cardiff

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