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For Companies At a Glance
- Tasks: Conduct site visits and ensure compliance in clinical research.
- Company: Join a leading global CRO trusted by top pharma and biotech firms.
- Benefits: Enjoy flexible home-based work and a competitive salary with great perks.
- Why this job: Make an impact on global health while enjoying a balanced travel schedule.
- Qualifications: 18-24 months CRA experience and a life sciences degree required.
- Other info: Opportunity to mentor junior CRAs and grow within a supportive team.
The predicted salary is between 36000 - 60000 £ per year.
Senior Clinical Research Associate – England
Chloe O\’Shea is proud to partner with a leading global CRO renowned for delivering innovative, high-quality solutions in clinical development. We are seeking an experienced Senior Clinical Research Associate (Senior CRA) to join a dedicated single-sponsor team in England. This is an exciting opportunity to work on cutting-edge studies, with a particular focus on advanced therapy areas such as CAR-T and gene therapy. While prior experience in these fields is highly valued, it is not essential – full training and support will be provided.
The Role
As a Senior CRA, you will be a key contributor to the successful delivery of clinical trials across England. You will oversee site management activities, act as a primary liaison with investigative sites, and ensure strict compliance with protocols, ICH-GCP, and UK regulatory requirements (MHRA/REC). This role is well-suited to ambitious CRAs ready to step up or established Senior CRAs seeking to deepen their expertise in innovative therapy areas.
Key Responsibilities
- Independently manage qualification, initiation, monitoring, and close-out visits across England.
- Ensure high standards of compliance with ICH-GCP, MHRA, REC requirements, and sponsor SOPs.
- Perform source data verification, investigational product accountability, and ensure accurate site documentation.
- Serve as a trusted partner to site personnel, offering training, guidance, and ongoing support.
- Identify site-level challenges proactively and drive timely resolution.
- Contribute to mentorship of junior CRAs and share best practices within the monitoring team.
- Maintain complete and accurate trial documentation in CTMS, eTMF, and EDC systems.
Requirements
- Bachelor\’s degree in Life Sciences, Nursing, Pharmacy, or a related discipline.
- Minimum 3 years of independent UK monitoring experience, ideally with exposure to complex studies.
- Experience in CAR-T and/or gene therapy is highly desirable but not required.
- Strong knowledge of ICH-GCP and UK clinical trial regulations (MHRA/REC).
- Excellent communication, relationship-building, and organisational skills.
What\’s in It for You?
This role offers a competitive salary and benefits package, flexible working arrangements, and clear opportunities for career progression within one of the world\’s largest CROs. You\’ll gain exposure to innovative therapies shaping the future of healthcare, while working in a collaborative culture that values professional development, work-life balance, and wellbeing.
If you are a driven Senior CRA — or an experienced CRA ready to take the next step — we\’d love to hear from you. Apply today to join a global team making a meaningful difference in patients\’ lives.
Senior Clinical Research Associate employer: AL Solutions
Contact Detail:
AL Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Clinical Research Associate
✨Tip Number 1
Network with professionals in the clinical research field. Attend industry conferences or local meetups to connect with current Senior Clinical Research Associates and learn about their experiences. This can provide you with valuable insights and potentially lead to referrals.
✨Tip Number 2
Familiarise yourself with the latest developments in ICH-GCP guidelines and UK regulations. Staying updated on these topics will not only enhance your knowledge but also demonstrate your commitment to compliance during interviews.
✨Tip Number 3
Prepare for potential interview questions by practising how you would handle specific site-related issues. Think of examples from your past experience where you successfully resolved problems, as this will showcase your problem-solving skills.
✨Tip Number 4
Highlight your multi-therapeutic area experience if applicable. If you've worked across various therapeutic areas, be ready to discuss how this diverse background can benefit the role and contribute to the company's goals.
We think you need these skills to ace Senior Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience as a Clinical Research Associate. Emphasise your independent monitoring experience, knowledge of ICH-GCP guidelines, and any multi-therapeutic area experience you have.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your commitment to advancing human health. Mention specific examples of how you've successfully conducted site visits and maintained compliance in previous roles.
Highlight Key Skills: In your application, clearly outline your communication, organisational, and problem-solving skills. Provide examples of how you've developed strong site relationships and resolved issues in past positions.
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 the role of a Senior Clinical Research Associate.
How to prepare for a job interview at AL Solutions
✨Know Your ICH-GCP Guidelines
As a Senior Clinical Research Associate, it's crucial to have a solid understanding of ICH-GCP guidelines. Brush up on these regulations before your interview, as you may be asked to discuss how you've applied them in your previous roles.
✨Demonstrate Your Monitoring Experience
With a minimum of 18–24 months’ independent monitoring experience required, be prepared to share specific examples from your past work. Highlight any challenges you faced during site visits and how you resolved them to showcase your problem-solving skills.
✨Showcase Your Communication Skills
Strong communication is key in this role. During the interview, practice articulating your thoughts clearly and confidently. You might also want to prepare examples of how you've built relationships with site staff to ensure compliance and performance.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's culture, the team you'll be working with, and the types of studies you'll be involved in. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.
