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For Companies At a Glance
- Tasks: Conduct site visits, monitor compliance, and mentor junior CRAs.
- Company: Join a leading global CRO trusted by top pharma and biotech firms.
- Benefits: Enjoy flexible home-based work, competitive salary, and career growth.
- Why this job: Make an impact on global studies while maintaining a balanced travel schedule.
- Qualifications: 18-24 months CRA experience, life sciences degree, and strong ICH-GCP knowledge.
- Other info: Opportunity to work in a supportive and collaborative environment.
The predicted salary is between 36000 - 60000 £ per year.
(SCRA) – UK (6–8 Site Visits/Month) – Global CRO
My client is a leading global Contract Research Organization (CRO), trusted by top pharmaceutical and biotech companies worldwide to deliver high-quality clinical research solutions. They are committed to advancing human health through innovation, collaboration, and scientific excellence.
The Opportunity
On behalf of my client, I am seeking an experienced Senior Clinical Research Associate (SCRA) to join their UK team. This position offers a balanced workload of 6–8 site visits per month, giving candidates the chance to work on impactful global studies while maintaining a sustainable travel schedule.
Key Responsibilities
- Conduct routine on-site monitoring visits in line with ICH-GCP, UK regulations, and sponsor SOPs.
- Develop and maintain strong site relationships to ensure high standards of performance and compliance.
- Perform source data verification (SDV), CRF review, and essential document checks.
- Identify and resolve site or protocol-related issues, escalating where required.
- Act as a resource and mentor for junior CRAs as needed.
Candidate Profile
- Minimum of 18–24 months’ independent monitoring experience as a CRA.
- Strong knowledge of ICH-GCP guidelines and UK regulatory environment.
- Multi-therapeutic area experience advantageous.
- Excellent communication, organizational, and problem-solving skills.
- Life sciences degree (or equivalent).
- Willingness to travel across the UK (6–8 site visits per month).
What’s on Offer
- Competitive salary and comprehensive benefits package.
- Flexible home-based working.
- Career progression opportunities within a global CRO.
- Supportive, collaborative working environment.
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 CRAs 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 by reviewing common challenges faced by CRAs. Think about how you would handle site-related issues or mentor junior staff, as this will showcase your problem-solving skills and leadership potential.
✨Tip Number 4
Research the company culture of the CRO you're applying to. Understanding their values and work environment can help you tailor your responses in interviews, showing that you’re a great fit for their team.
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
Make sure you have a solid understanding of the ICH-GCP guidelines and UK regulations. Be prepared to discuss how you've applied these in your previous roles, as this will demonstrate your expertise and commitment to compliance.
✨Showcase Your Monitoring Experience
Highlight your independent monitoring experience, especially any specific challenges you've faced and how you overcame them. This will help the interviewer see your problem-solving skills in action.
✨Emphasise Relationship Building
Since developing strong site relationships is key, be ready to share examples of how you've successfully built rapport with sites in the past. This shows that you understand the importance of collaboration in clinical research.
✨Prepare for Scenario Questions
Expect scenario-based questions where you might need to identify and resolve site or protocol-related issues. Practising these types of questions can help you articulate your thought process clearly during the interview.
