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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, flexible hybrid working, and a supportive team environment.
- Why this job: Be part of a dynamic team making a real impact in patients' lives through clinical research.
- Qualifications: 4-5 years of CRA experience with essential site monitoring skills required.
- Other info: Work on diverse clinical projects in a collaborative atmosphere.
The predicted salary is between 36000 - 60000 £ per year.
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.
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.
- 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.
- 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. Competitive compensation package. Flexible hybrid working model. Opportunity to work in a supportive and professional environment with diverse clinical projects.
(Senior) Clinical Research Associate - Pharmaceuticals employer: EPM Scientific
Contact Detail:
EPM Scientific Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land (Senior) Clinical Research Associate - Pharmaceuticals
✨Tip Number 1
Network with professionals in the clinical research field, especially those who are currently working as Clinical Research Associates. Attend industry conferences or local meetups to connect with potential colleagues and learn about their experiences at companies like ours.
✨Tip Number 2
Familiarise yourself with the latest trends and regulations in clinical trials, particularly ICH-GCP guidelines. This knowledge will not only enhance your understanding but also demonstrate your commitment to staying updated in this fast-evolving field.
✨Tip Number 3
Prepare for the interview by practising common CRA scenarios, such as how to handle site monitoring challenges or resolve compliance issues. Being able to discuss real-life examples will showcase your problem-solving skills and experience.
✨Tip Number 4
Research our company’s recent projects and therapeutic areas we focus on. Understanding our mission and values will help you align your answers during the interview and show that you’re genuinely interested in contributing to our goals.
We think you need these skills to ace (Senior) Clinical Research Associate - Pharmaceuticals
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience as a Clinical Research Associate, particularly your site monitoring skills. Emphasise your 4-5 years of CRA experience and any specific achievements in clinical trials.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for pharmaceuticals and your understanding of the company's mission. Mention your experience with regulatory requirements and how you can contribute to their innovative therapies.
Highlight Relevant Skills: In your application, clearly outline your skills related to on-site monitoring, problem-solving at clinical sites, and collaboration with project teams. Use specific examples to demonstrate your expertise.
Proofread Your Application: Before submitting, carefully proofread your application 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 examples of how you've conducted initiation, routine, and close-out visits, as well as any challenges you faced and how you resolved them.
✨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 and how you handle any issues that arise at clinical sites.
✨Emphasise Collaboration Skills
Since the role involves cross-functional collaboration, be ready to share examples of how you've worked effectively with project teams in the past. Highlight your communication skills and ability to work in a dynamic environment.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving abilities. Think about situations where you had to identify and resolve issues at clinical sites, and be ready to explain your thought process and actions taken.
