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- Tasks: Monitor Oncology clinical trials and ensure compliance with protocols and regulations.
- Company: Global clinical research organisation dedicated to improving patient outcomes.
- Benefits: Opportunities for professional development and a long-term career in clinical research.
- Other info: Flexible travel across the UK and collaboration with diverse study teams.
- Why this job: Make a real impact on patient lives while developing your expertise in a dynamic environment.
- Qualifications: Experience in monitoring Oncology trials and strong knowledge of GCP regulations.
The predicted salary is between 35000 - 45000 £ per year.
An established global clinical research organisation is seeking a Clinical Research Associate (CRA) to join its Site Management (multi-sponsor) team, supporting Oncology clinical trials across the UK. This role offers the opportunity to contribute to meaningful research that improves patient outcomes, while continuing to develop your monitoring expertise in a high-quality, regulated environment.
Key Responsibilities
- Conduct site monitoring visits (selection, initiation, routine monitoring, and close-out) in line with contracted scope and Good Clinical Practice (GCP).
- Support Oncology studies, ensuring protocol compliance and data integrity.
- Partner with investigational sites to drive, adapt, and track patient recruitment plans.
- Deliver protocol and study-specific training and maintain regular communication with sites.
- Assess site quality and compliance with protocols, regulations, and ethical standards, escalating issues where required.
- Track study progress including regulatory submissions, approvals, enrolment, CRF completion, and data query resolution.
- Ensure accurate and compliant maintenance of the Trial Master File (TMF) and Investigator Site File (ISF).
- Prepare clear and timely monitoring visit reports, follow-up letters, and action plans.
- Collaborate closely with cross-functional study team members to support delivery milestones.
Requirements
- Proven experience independently monitoring Oncology clinical trials, including unblinded studies.
- Strong working knowledge of ICH-GCP and applicable regulatory requirements.
- Degree in Life Sciences or equivalent industry experience.
- Flexibility and willingness to travel to sites across the UK.
- Strong organisational, communication, and stakeholder-management skills.
Why Apply
- Work on impactful Oncology studies.
- Exposure to multi-sponsor trials and diverse site environments.
- Strong focus on quality, learning, and professional development.
- Opportunity to build a long-term career in clinical research.
Clinical Research Associate employer: SoTalent
Contact Detail:
SoTalent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field, especially those working in oncology. Attend industry events or webinars, and don’t be shy about asking for informational interviews. We all know that sometimes it’s not just what you know, but who you know!
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ICH-GCP and regulatory requirements. We recommend practising common interview questions related to site monitoring and patient recruitment. Show them you’re not just a candidate, but the candidate they’ve been looking for!
✨Tip Number 3
Don’t forget to follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. We suggest mentioning something specific from your conversation to make it personal and memorable.
✨Tip Number 4
Apply through our website for the best chance at landing that Clinical Research Associate role. We’re always on the lookout for passionate individuals ready to make a difference in oncology research. Let’s get you started on this exciting journey!
We think you need these skills to ace Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Research Associate role. Highlight your experience in monitoring Oncology clinical trials and any relevant qualifications. We want to see how your background aligns with what we’re looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about Oncology research and how your skills can contribute to our team. Keep it concise but impactful – we love a good story!
Showcase Your Skills: Don’t forget to highlight your organisational and communication skills in your application. These are key for a CRA role, especially when managing multiple sites and ensuring protocol compliance. Let us know how you’ve excelled in these areas!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just a few clicks and you’re done!
How to prepare for a job interview at SoTalent
✨Know Your Oncology Stuff
Make sure you brush up on your knowledge of oncology clinical trials. Familiarise yourself with the latest trends, challenges, and regulations in the field. This will not only show your passion but also demonstrate that you're serious about contributing to meaningful research.
✨Master GCP and Regulatory Requirements
Since this role requires a strong working knowledge of ICH-GCP and regulatory requirements, be prepared to discuss these in detail. We recommend reviewing key guidelines and being ready to explain how you've applied them in your previous roles.
✨Showcase Your Monitoring Experience
Be ready to share specific examples from your past experiences where you successfully conducted site monitoring visits. Highlight your ability to ensure protocol compliance and data integrity, as well as any challenges you faced and how you overcame them.
✨Communicate Effectively
Strong communication skills are essential for this role. Practice articulating your thoughts clearly and concisely. During the interview, engage with your interviewers by asking insightful questions about their studies and how you can contribute to their goals.