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- Tasks: Monitor clinical trials, ensuring compliance with regulations and protocols.
- Company: Join a mission-driven team dedicated to developing life-changing therapies.
- Benefits: Enjoy competitive pay, professional development, and a collaborative work environment.
- Why this job: Make a real impact in healthcare while growing your career in a supportive setting.
- Qualifications: 1 year of monitoring experience; strong communication and problem-solving skills required.
- Other info: Must be UK-based and able to work on-site in West London 2 days a week.
The predicted salary is between 36000 - 60000 £ per year.
We are seeking a motivated and detail-oriented Junior Clinical Research Associate (CRA) to join our team. This is an excellent opportunity for someone with at least one year of on-site monitoring experience, ideally gained within a CRO environment. The successful candidate will be responsible for monitoring clinical trials to ensure compliance with regulatory requirements, Good Clinical Practice (GCP), and study protocols.
Key Responsibilities
- Conduct on-site and remote monitoring visits to ensure compliance with study protocols, GCP, and regulatory requirements.
- Perform source data verification and ensure data accuracy and completeness.
- Build and maintain strong relationships with site staff to support study conduct and patient recruitment.
- Identify and resolve site-level issues, escalating as needed.
- Prepare and submit monitoring visit reports and follow-up documentation in a timely manner.
- Collaborate with internal teams to support study timelines and deliverables.
Requirements
- Minimum 1 year of independent monitoring experience in a clinical research setting.
- Experience working within a CRO or similar environment is acceptable.
- Strong understanding of ICH-GCP and clinical trial regulations.
- Excellent communication, organizational, and problem-solving skills.
- Ability to work independently and manage multiple priorities.
- Must be UK-based and able to work on-site in West London 2 days per week.
- Willingness to travel for site visits as required.
Preferred Qualifications
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- Experience across multiple therapeutic areas is welcome but not essential.
Why Join Us?
- Competitive compensation and benefits package.
- Work with a collaborative, mission-driven team.
- Opportunities for professional development and internal growth.
- Contribute directly to the development of life-changing therapies.
Clinical Research Associate (CRA) (London) employer: EPM Scientific
Contact Detail:
EPM Scientific Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate (CRA) (London)
✨Tip Number 1
Network with professionals in the clinical research field, especially those who work in CROs. Attend industry events or webinars to connect with potential colleagues and learn more about the role.
✨Tip Number 2
Familiarise yourself with the latest ICH-GCP guidelines and clinical trial regulations. This knowledge will not only boost your confidence but also demonstrate your commitment to compliance during interviews.
✨Tip Number 3
Prepare to discuss specific examples from your previous monitoring experience. Highlight how you resolved site-level issues or improved data accuracy, as this will showcase your problem-solving skills.
✨Tip Number 4
Research StudySmarter's current projects and values. Understanding our mission and how you can contribute will help you articulate why you're a great fit for the team during any discussions.
We think you need these skills to ace Clinical Research Associate (CRA) (London)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in clinical research, particularly any on-site monitoring roles. Emphasise your understanding of GCP and regulatory requirements, as well as any specific therapeutic areas you've worked in.
Craft a Strong Cover Letter: Write a cover letter that showcases your motivation for the role and your passion for clinical research. Mention your experience in a CRO environment and how it has prepared you for this position. Be sure to address why you want to work with this specific company.
Highlight Key Skills: In your application, clearly outline your communication, organisational, and problem-solving skills. Provide examples of how you've successfully managed multiple priorities or resolved site-level 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 in clinical research.
How to prepare for a job interview at EPM Scientific
✨Know Your GCP and Regulations
Brush up on your knowledge of Good Clinical Practice (GCP) and ICH guidelines. Being able to discuss these regulations confidently will show that you understand the framework within which you'll be working.
✨Demonstrate Your Monitoring Experience
Prepare specific examples from your previous monitoring experience. Highlight how you ensured compliance during trials and any challenges you faced, along with how you resolved them.
✨Showcase Your Communication Skills
Since building relationships with site staff is crucial, be ready to discuss how you've effectively communicated in past roles. Share instances where your communication skills helped resolve issues or improved collaboration.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's clinical trials and their approach to patient recruitment. This shows your genuine interest in the role and helps you assess if the company aligns with your career goals.
