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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 of CRA experience with strong site monitoring skills 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.
- 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.
- 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 to hearing from you!
Senior Clinical Research Associate (Senior CRA) 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)
✨Tip Number 1
Network with professionals in the clinical research field, especially those who work in or have connections to West London. Attend industry events or webinars to meet potential colleagues and learn more about the company culture.
✨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 but also demonstrate your commitment to staying updated in the field.
✨Tip Number 3
Prepare to discuss specific examples from your previous CRA experience that highlight your problem-solving skills and ability to build strong site relationships. Real-life scenarios can make a significant impact during interviews.
✨Tip Number 4
Research the company's recent projects and therapeutic areas they focus on. Being knowledgeable about their work will help you tailor your conversation and show genuine interest during the interview process.
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 responsibilities outlined in 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 has prepared you for this role, particularly in relation to site monitoring and regulatory compliance.
Highlight Key Skills: In your application, clearly outline your excellent communication and problem-solving skills. Provide examples of how you've built strong 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
✨Showcase Your Monitoring Experience
Make sure to 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 demonstrate your hands-on expertise and problem-solving skills.
✨Understand Regulatory Requirements
Familiarise yourself with ICH-GCP guidelines and other regulatory requirements relevant to clinical trials. Be prepared to discuss how you ensure compliance in your previous roles, as this is crucial for the position.
✨Build Rapport with Interviewers
Since building strong site relationships is key in this role, use the interview to establish a connection with your interviewers. Show your interpersonal skills and ability to collaborate effectively with cross-functional teams.
✨Prepare Questions About the Company
Research the company’s focus on rare and underserved conditions. Prepare thoughtful questions about their projects and how you can contribute to their mission. This shows your genuine interest in the role and the organisation.
