Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- 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 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 events or webinars to connect with potential colleagues and learn more about the role.
✨Tip Number 2
Familiarise yourself with the latest regulations and guidelines related to GCP and ICH. 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 issues at sites and maintained relationships with site staff, as these are crucial skills for a CRA.
✨Tip Number 4
Show your enthusiasm for the role by researching StudySmarter and understanding our mission. Tailor your conversations to reflect how your values align with ours, which can make a strong impression during interviews.
We think you need these skills to ace Clinical Research Associate (CRA
Some tips for your application 🫡
Understand the Role: Before applying, make sure to thoroughly read the job description for the Clinical Research Associate position. Understand the key responsibilities and requirements to tailor your application accordingly.
Highlight Relevant Experience: In your CV and cover letter, emphasise your on-site monitoring experience, especially if it was gained within a CRO environment. Be specific about your roles and achievements in previous positions.
Showcase Your Skills: Clearly demonstrate your understanding of ICH-GCP and clinical trial regulations in your application. Use examples to illustrate your communication, organisational, and problem-solving skills.
Personalise Your Application: Address your cover letter to the hiring manager if possible, and express why you are specifically interested in this role and company. Mention how your values align with their mission-driven approach.
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 how you've applied them in previous roles.
✨Demonstrate Your Monitoring Experience
Highlight your on-site monitoring experience during the interview. Be ready to share specific examples of how you've conducted monitoring visits, performed source data verification, and resolved site-level issues.
✨Showcase Your Communication Skills
As a CRA, building relationships with site staff is crucial. Prepare to discuss how you've effectively communicated with different stakeholders in past roles and how you handle challenging conversations.
✨Prepare Questions About the Role
Show your interest in the position by preparing thoughtful questions about the company's clinical trials, team dynamics, and opportunities for professional development. This demonstrates your enthusiasm and helps you assess if the role is a good fit for you.
