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- Tasks: Conduct site monitoring visits and ensure compliance with clinical trial protocols.
- Company: Join a global pharmaceutical company focused on innovative therapies for rare conditions.
- Benefits: Enjoy a competitive salary and flexible hybrid working model.
- Why this job: Be part of a dynamic team making a real impact in patients' lives.
- Qualifications: 4-5 years of CRA experience with essential on-site monitoring skills.
- Other info: Work in a supportive environment with diverse clinical projects.
The predicted salary is between 43200 - 72000 £ per year.
About Us: We are a global specialty pharmaceutical company dedicated to improving the lives of patients through the development of innovative and targeted therapies. Our focus is on addressing unmet medical needs, particularly in rare and underserved conditions. We offer a collaborative and dynamic work environment where clinical research professionals are empowered to contribute meaningfully.
About the Role: We are seeking an experienced Senior Clinical Research Associate (Snr CRA) to join a dynamic team based in West London. This role requires a strong background in site monitoring, with regular on-site presence (2 days/week). The ideal candidate will bring a minimum of 4-5 years of CRA experience, with a solid understanding of clinical trial processes and regulatory requirements.
Key Responsibilities:
- Conduct on-site monitoring visits, including initiation, routine, and close-out visits.
- Ensure trials are conducted, recorded, and reported in accordance with the protocol, SOPs, ICH-GCP, and applicable regulatory requirements.
- Build and maintain strong site relationships.
- Identify and resolve issues at clinical sites to ensure data quality and compliance.
- Prepare monitoring visit reports and follow up on action items.
- Collaborate cross-functionally with project teams.
Requirements:
- 4-5 years of experience as a Clinical Research Associate.
- Must have been a site monitor - on-site monitoring experience is essential.
- Proven ability to work independently with minimal oversight.
- Excellent communication and problem-solving skills.
- Flexibility across therapeutic areas (no specific experience required).
- Based within commutable distance to West London.
Why Join Us?
- Competitive compensation package.
- Flexible hybrid working model.
- Opportunity to work in a supportive and professional environment with diverse clinical projects.
To Apply: If you are interested please submit your CV - look forward hearing from you!
Senior Clinical Research Associate (Senior CRA) (London) employer: EPM Scientific
Contact Detail:
EPM Scientific Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Research Associate (Senior CRA) (London)
✨Tip Number 1
Network with professionals in the clinical research field, especially those who are currently working as Clinical Research Associates. Attend industry events or webinars to connect with potential colleagues and learn more about the company culture at StudySmarter.
✨Tip Number 2
Familiarise yourself with the latest trends and regulations in clinical trials, particularly ICH-GCP guidelines. This knowledge will not only boost your confidence during interviews but also demonstrate your commitment to staying updated in the field.
✨Tip Number 3
Prepare specific examples from your previous experience that showcase your site monitoring skills and problem-solving abilities. Be ready to discuss how you've successfully managed challenges at clinical sites in past roles.
✨Tip Number 4
Research StudySmarter's recent projects and therapeutic areas they focus on. Tailoring your conversation to reflect an understanding of their work can help you stand out as a candidate who is genuinely interested in contributing to their mission.
We think you need these skills to ace Senior Clinical Research Associate (Senior CRA) (London)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience as a Clinical Research Associate, particularly your on-site monitoring experience. Use specific examples that demonstrate your understanding of clinical trial processes and regulatory requirements.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your passion for improving patient lives through innovative therapies. Mention why you are interested in this specific role and how your skills align with the company's mission.
Highlight Key Skills: In your application, emphasise your problem-solving abilities and communication skills. Provide examples of how you've successfully built relationships at clinical sites and resolved issues to ensure data quality and compliance.
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 Clinical Trial Processes
Make sure you have a solid understanding of clinical trial processes and regulatory requirements. Brush up on ICH-GCP guidelines and be ready to discuss how you've applied these in your previous roles.
✨Demonstrate Your Monitoring Experience
Since on-site monitoring experience is essential, prepare specific examples from your past roles where you successfully conducted monitoring visits. Highlight any challenges you faced and how you resolved them.
✨Showcase Your Communication Skills
Strong communication skills are crucial for this role. Be prepared to discuss how you've built and maintained relationships with site staff and project teams. Consider sharing anecdotes that illustrate your ability to communicate effectively.
✨Be Ready for Problem-Solving Scenarios
Expect questions that assess your problem-solving abilities. Think of situations where you identified issues at clinical sites and how you addressed them. This will demonstrate your proactive approach and ability to ensure data quality and compliance.
