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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 organisational 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 30000 - 42000 £ 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 employer: EPM Scientific
Contact Detail:
EPM Scientific Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate (CRA
✨Tip Number 1
Network with professionals in the clinical research field, especially those who work in CROs. Attend industry conferences or local meetups to connect with potential colleagues and learn about job openings.
✨Tip Number 2
Familiarise yourself with the latest regulations and guidelines related to clinical trials, such as ICH-GCP. This knowledge will not only boost your confidence but also demonstrate your commitment to compliance during interviews.
✨Tip Number 3
Prepare for the interview by practising common CRA scenarios, such as how to handle site-level issues or improve patient recruitment. Being able to discuss real-life examples 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 your discussions with us.
We think you need these skills to ace Clinical Research Associate (CRA
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience, especially any on-site monitoring roles you've held. Emphasise your understanding of GCP and clinical trial regulations, as these are crucial for the role.
Craft a Strong Cover Letter: In your cover letter, express your motivation for applying to this specific position. Mention your experience in a CRO environment and how it has prepared you for the responsibilities outlined in the job description.
Showcase Communication Skills: Since excellent communication is key for this role, consider including examples in your application that demonstrate your ability to build relationships with site staff and resolve issues effectively.
Highlight Problem-Solving Abilities: Provide specific examples of challenges you've faced in previous roles and how you successfully addressed them. This will showcase your problem-solving skills, which are essential for a Clinical Research Associate.
How to prepare for a job interview at EPM Scientific
✨Know Your GCP and ICH Guidelines
Make sure you have a solid understanding of Good Clinical Practice (GCP) and the International Council for Harmonisation (ICH) guidelines. Be prepared to discuss how these regulations impact your work and provide examples from your previous experience.
✨Demonstrate Your Monitoring Experience
Highlight your on-site monitoring experience during the interview. Discuss specific trials you've worked on, the challenges you faced, and how you overcame them. This will show your practical knowledge and problem-solving skills.
✨Build Rapport with Site Staff
Emphasise your ability to build strong relationships with site staff. Share examples of how you've successfully collaborated with others to support study conduct and patient recruitment, as this is crucial for the role.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your critical thinking and decision-making skills. Prepare by thinking through potential site-level issues you might encounter and how you would address them effectively.
