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For Companies 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 with great perks.
- Why this job: Make an impact on global health while enjoying a balanced travel schedule.
- Qualifications: 18-24 months CRA experience, life sciences degree, and strong ICH-GCP knowledge required.
- Other info: Opportunity to mentor junior CRAs and grow within a supportive team.
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 you with 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 during interviews. Think about past experiences where you successfully resolved site-related issues or mentored junior staff, as these examples will showcase your problem-solving skills and leadership abilities.
✨Tip Number 4
Research the company culture of the CRO you're applying to. Understanding their values and mission can help you tailor your responses in interviews, showing that you align with their goals and are genuinely interested in contributing to their success.
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 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 their needs, particularly your ability to conduct site visits and maintain compliance.
Showcase Your Communication Skills: In your application, provide examples of how you've developed strong relationships with sites and resolved issues. This will demonstrate your excellent communication and problem-solving skills, which are crucial for this role.
Highlight Your Educational Background: Mention your life sciences degree or equivalent qualifications prominently in your application. This is a key requirement for the position, so ensure it stands out.
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 illustrate your problem-solving skills and ability to manage site relationships effectively.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your decision-making and conflict resolution skills. Think of examples from your past experiences where you successfully identified and resolved site or protocol-related issues.
✨Emphasise Communication Skills
As a Senior Clinical Research Associate, strong communication is key. Be ready to discuss how you've built relationships with sites and mentored junior CRAs, showcasing your ability to collaborate and lead within a team.
