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- Tasks: Conduct on-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 as a Clinical Research Associate with site monitoring experience required.
- Other info: Position based in West London; must be within commuting distance.
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!
Contact Detail:
EPM Scientific Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Research Associate (Senior CRA)
✨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. Being knowledgeable about ICH-GCP guidelines and recent changes in regulatory requirements will demonstrate your commitment and expertise during interviews.
✨Tip Number 3
Prepare specific examples from your previous experience that highlight your site monitoring skills and problem-solving abilities. Be ready to discuss how you've built relationships with sites and resolved issues effectively.
✨Tip Number 4
Research StudySmarter's current projects and therapeutic areas they focus on. Showing genuine interest in their work and aligning your experience with their needs can set you apart from other candidates.
We think you need these skills to ace Senior Clinical Research Associate (Senior CRA)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience as a Clinical Research Associate. Emphasise your site monitoring experience and any specific achievements in previous roles that align with the job description.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of the company's mission. Mention your 4-5 years of CRA experience and how it prepares you for this role, particularly in relation to site monitoring.
Highlight Key Skills: In your application, clearly outline your problem-solving skills and ability to work independently. Provide examples of how you've built strong relationships at clinical sites and resolved issues to ensure data quality.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or typos. A polished application reflects your attention to detail, which is crucial in clinical research.
How to prepare for a job interview at EPM Scientific
✨Showcase Your Monitoring Experience
Make sure to highlight your on-site monitoring experience during the interview. Discuss specific examples of how you've conducted initiation, routine, and close-out visits, as this is crucial for the Senior CRA role.
✨Demonstrate Problem-Solving Skills
Prepare to discuss situations where you've identified and resolved issues at clinical sites. This will showcase your ability to ensure data quality and compliance, which is a key responsibility in this position.
✨Emphasise Communication Abilities
Since building strong site relationships is essential, be ready to talk about how you communicate effectively with site staff and project teams. Share examples that demonstrate your excellent communication skills.
✨Understand Regulatory Requirements
Brush up on ICH-GCP guidelines and other regulatory requirements relevant to clinical trials. Being able to discuss these in detail will show your solid understanding of the clinical trial processes expected for this role.
