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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: Opportunity for professional development and a long-term career in clinical research.
- Why this job: Make a real impact on patient lives through meaningful research.
- Qualifications: Experience in monitoring Oncology trials and strong knowledge of GCP regulations.
- Other info: Flexible travel across the UK and collaborative team environment.
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 in Brighton employer: SoTalent
Contact Detail:
SoTalent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate in Brighton
✨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 to make connections and learn about potential job openings.
✨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 to showcase your expertise.
✨Tip Number 3
Showcase your flexibility and willingness to travel during interviews. Highlight any previous experiences where you successfully managed multiple sites or adapted to changing circumstances in clinical trials.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are genuinely interested in joining our team.
We think you need these skills to ace Clinical Research Associate in Brighton
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!
Showcase Your Skills: Don’t just list your skills; demonstrate them! Use specific examples from your past experiences that showcase your organisational, communication, and stakeholder-management skills. This will help us see how you can contribute to our team.
Be Clear and Concise: When writing your application, clarity is key. Keep your language straightforward and avoid jargon unless it’s necessary. We appreciate a well-structured application that gets straight to the point!
Apply Through Our Website: We encourage you to apply through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to find all the details you need about the role and our company!
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 heavily involves Good Clinical Practice (GCP), ensure you can discuss it confidently. Be prepared to answer questions about ICH-GCP guidelines and how they apply to site monitoring. This will highlight your expertise and readiness for the role.
✨Showcase Your Organisational Skills
As a Clinical Research Associate, you'll need to juggle multiple tasks. Prepare examples from your past experiences where you've successfully managed your time and resources. This will help illustrate your ability to handle the responsibilities of the role effectively.
✨Engage with the Interviewers
Don't just wait for questions; engage with your interviewers! Ask insightful questions about their current studies or challenges they face. This shows your interest in the role and helps you assess if the company is the right fit for you.