Senior CRA

Senior Clinical Research Associate (Oncology) - UK

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.

• 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 elevate 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

• 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)

• 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

• 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

• Number of studies: approximately 1-3
• Number of sites: 4-7
• Site locations include:
  Manchester, London, Glasgow, Liverpool, Sheffield, and Cardiff

• 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