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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 in Oncology.
- Qualifications: Experience in monitoring clinical trials and a degree in Life Sciences.
- Other info: Flexible travel across the UK and exposure to diverse site environments.
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 Eastbourne employer: SoTalent
Contact Detail:
SoTalent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate in Eastbourne
✨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. Be ready to discuss your experience with monitoring clinical trials and how you ensure protocol compliance.
✨Tip Number 3
Showcase your organisational skills! During interviews, highlight how you manage multiple tasks, track study progress, and maintain accurate documentation. This will demonstrate your ability to handle the responsibilities of a CRA.
✨Tip Number 4
Don’t forget to apply through our website! We’ve got loads of opportunities waiting for you, and applying directly can give you an edge over other candidates. Plus, it’s super easy!
We think you need these skills to ace Clinical Research Associate in Eastbourne
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, treatments, and challenges 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 Regulations
Since this role requires a strong working knowledge of ICH-GCP and regulatory requirements, we suggest you review these guidelines thoroughly. Be prepared to discuss how you've applied these principles in your previous roles, as this will highlight your expertise and readiness for the position.
✨Showcase Your Monitoring Experience
Prepare specific examples from your past experiences where you successfully conducted site monitoring visits. Discuss how you ensured protocol compliance and data integrity, as well as any challenges you faced and how you overcame them. This will help illustrate your hands-on experience and problem-solving skills.
✨Communicate Effectively
Strong communication skills are key in this role, so practice articulating your thoughts clearly and confidently. Think about how you would explain complex concepts to different stakeholders, including investigational sites. This will demonstrate your ability to collaborate effectively and maintain strong relationships.