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- Tasks: Support oncology clinical trials through site monitoring and compliance checks.
- Company: Join a dynamic team focused on advancing cancer research.
- Benefits: Enjoy hybrid work flexibility and gain valuable hands-on experience.
- Why this job: Perfect for early-career professionals eager to make an impact in oncology.
- Qualifications: Bachelor’s degree in Life Sciences or related field; 1-2 years of clinical research experience.
- Other info: Opportunity to participate in training sessions and collaborate with industry experts.
The predicted salary is between 36000 - 60000 £ per year.
Clinical Research Associate II (CRA II) Location: Remote (UK-based) Contract: Full-time, permanent Start Date: April–June 2026 Travel: UK site visits approximately every 6–8 weeks (with potential for future global travel) Our client is a growing, ISO 9001–certified CRO delivering high-quality clinical research across Non-Interventional studies, CTIMPs, ATMPs, Rare Disease, and Medical Device investigations . Due to internal progression and a strong upcoming pipeline, they are seeking an experienced CRA II to join their collaborative clinical operations team. The Role The CRA II will act as the primary point of contact for clinical sites, ensuring trial delivery is compliant, high quality, and on schedule. The role involves monitoring multi-centre trials across various therapeutic areas and phases, supporting sites throughout the full study lifecycle, and contributing to continuous improvement initiatives. Key Responsibilities Site selection, initiation, monitoring, and close-out Monitoring multi-centre clinical trials across multiple phases Delivering site initiation training and ongoing site support CRF review, SDV, and data quality oversight Tracking recruitment, compliance, and study progress Preparing monitoring reports and follow-up documentation Escalating protocol deviations and serious breaches Supporting ethics and regulatory submissions Collaborating with project teams to maintain trial quality Candidate Profile 2–3+ years’ experience as a CRA (CRA I or II) Experience monitoring multi-centre clinical trials (oncology experience preferred) Exposure across Phase I–IV studies Degree in a life sciences or related discipline Strong knowledge of ICH-GCP Excellent communication and organisational skills Right to work in the UK, full UK driving licence, and valid passport What’s On Offer Remote-first working model Supportive, collaborative culture Strong focus on learning and professional development Private medical insurance and performance-related bonus Generous annual leave and wellbeing initiatives This opportunity is ideal for a proactive, quality-driven CRA looking to grow within a supportive CRO environment.
Clinical Research Associate employer: Barrington James
Contact Detail:
Barrington James Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate
✨Tip Number 1
Network with professionals in the oncology field. Attend industry conferences, webinars, or local meetups to connect with Clinical Research Associates and other experts. This can help you gain insights into the role and potentially lead to referrals.
✨Tip Number 2
Familiarise yourself with the latest trends and developments in oncology clinical trials. Follow relevant journals, blogs, and social media channels to stay updated. This knowledge can be a great conversation starter during interviews.
✨Tip Number 3
Consider reaching out to current or former Clinical Research Associates at StudySmarter. They can provide valuable insights about the company culture and expectations, which can help you tailor your approach when applying.
✨Tip Number 4
Prepare for potential interview questions by practising your responses to common scenarios faced by Clinical Research Associates. Think about how you would handle site monitoring visits or resolve compliance issues, as these are key aspects of the role.
We think you need these skills to ace Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical research, particularly any exposure to oncology trials. Emphasise your educational background in Life Sciences, Nursing, or Pharmacy, and include any internships or roles that demonstrate your understanding of ICH-GCP guidelines.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for oncology and clinical trials. Mention specific experiences that align with the responsibilities listed in the job description, such as site monitoring visits or supporting site staff with compliance.
Highlight Relevant Skills: In your application, clearly outline your organisational skills, attention to detail, and ability to manage multiple tasks. Provide examples of how you've successfully communicated with teams or resolved issues in previous roles.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a Clinical Research Associate role.
How to prepare for a job interview at Barrington James
✨Know Your Oncology Basics
Make sure you brush up on your knowledge of oncology clinical trials. Understand the key terms and processes involved, as this will show your passion for the field and your readiness to contribute.
✨Demonstrate Attention to Detail
As a Clinical Research Associate, attention to detail is crucial. Be prepared to discuss examples from your past experiences where your meticulous nature helped resolve issues or improve processes.
✨Familiarise Yourself with ICH-GCP Guidelines
Since compliance with regulatory guidelines is a big part of the role, make sure you can confidently discuss ICH-GCP guidelines. This will demonstrate your understanding of the standards expected in clinical research.
✨Prepare Questions for the Interviewers
Show your enthusiasm and interest by preparing thoughtful questions about the company’s oncology projects, team dynamics, and expectations for the role. This not only helps you gauge if it’s the right fit but also leaves a positive impression.
