Senior Clinical Research Associate
Senior Clinical Research Associate

Senior Clinical Research Associate

Bournemouth Full-Time 42000 - 84000 Β£ / year (est.) No home office possible
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At a Glance

  • Tasks: Conduct site visits and monitor clinical research compliance.
  • Company: Join a leading global CRO trusted by top pharma and biotech firms.
  • Benefits: Enjoy flexible home-based work and a competitive salary.
  • Why this job: Make an impact on global health while developing your career in a supportive team.
  • Qualifications: 18-24 months CRA experience and a life sciences degree required.
  • Other info: Opportunity for mentorship and travel across the UK.

The predicted salary is between 42000 - 84000 Β£ 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 β€” or an experienced CRA ready to take the next step β€” 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

As a leading global Contract Research Organization, our client offers an exceptional work environment for Senior Clinical Research Associates, characterised by a commitment to innovation and scientific excellence. Employees benefit from a competitive salary, a comprehensive benefits package, and flexible home-based working arrangements, all while engaging in meaningful global studies that advance human health. With ample opportunities for career progression and a supportive, collaborative culture, this role is ideal for those seeking to make a significant impact in the clinical research field.
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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 valuable insights and potentially lead to referrals.

✨Tip Number 2

Familiarise yourself with the latest ICH-GCP guidelines and UK regulations. Being well-versed in these areas will not only boost your confidence but also demonstrate your commitment to compliance during interviews.

✨Tip Number 3

Prepare for potential scenario-based questions that may arise during interviews. Think of examples from your past experience where you successfully resolved site-related issues or mentored junior CRAs, as this will showcase your problem-solving skills and leadership abilities.

✨Tip Number 4

Research the company culture of the global CRO you're applying to. Understanding their values and work environment can help you tailor your responses in interviews, showing that you are a good fit for their team.

We think you need these skills to ace Senior Clinical Research Associate

Independent Monitoring Experience
Knowledge of ICH-GCP Guidelines
Understanding of UK Regulatory Environment
Source Data Verification (SDV)
CRF Review
Essential Document Checks
Site Relationship Management
Problem-Solving Skills
Organisational Skills
Communication Skills
Mentoring Skills
Multi-Therapeutic Area Experience
Willingness to Travel
Attention to Detail

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 Strong Cover Letter: Write a cover letter that specifically addresses the key responsibilities mentioned in the job description. Explain how your skills and experiences align with the company's commitment to high-quality clinical research solutions.

Highlight Your Soft Skills: In your application, showcase your excellent communication, organisational, and problem-solving skills. Provide examples of how you've developed strong site relationships and resolved issues in previous roles.

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 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 18–24 months of 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 it's the right fit for you.

Senior Clinical Research Associate
AL Solutions
Location: Bournemouth
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  • Senior Clinical Research Associate

    Bournemouth
    Full-Time
    42000 - 84000 Β£ / year (est.)
  • A

    AL Solutions

    50-100
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