Senior Clinical Research Associate

Cpl; England; Hybrid; GBP 50,000 - 65,000; Full time

Job summary

A specialized oncology group is seeking an experienced Senior Clinical Research Associate to support Phase I to III studies across the UK. The role requires confident on site monitoring, strong RECIST experience, and a solid understanding of early phase oncology. You will travel across the UK, perform on site monitoring, and manage relationships while ensuring compliance with regulations. The ideal candidate should have at least five years of CRA experience in oncology and ideally be fluent in Spanish.

Qualifications

• At least five years of CRA on site monitoring in oncology.
• Strong RECIST experience required.
• Experience in Phase I to III monitoring is essential.

Responsibilities

• Perform on site monitoring across four to seven UK sites.
• Review safety, tumour assessments and adverse events.
• Ensure full compliance with ICH GCP.

Skills

On site monitoring

RECIST criteria application

Fluent English

Strong communication skills

Job description

Senior Clinical Research Associate Oncology

Field based with travel across major UK clinical sites

A specialist oncology group is seeking an experienced Senior CRA to support Phase I to III studies across the UK. This position requires confident on site monitoring, RECIST experience and a strong understanding of early phase oncology.

What you will do

• Perform on site monitoring across four to seven UK sites
• Review safety, tumour assessments and adverse events
• Apply RECIST criteria in tumour response evaluation
• Ensure full compliance with ICH GCP
• Manage site relationships and resolve study issues
• Travel six to seven days per month

What you need

• At least five years of CRA on site monitoring in oncology
• Strong RECIST experience
• Phase I to III monitoring background
• Fluent English and ideally Spanish
• Ability to travel across the UK and stay overnight when required
• Based within one hour of a major airport or rail hub