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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 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
Research the company culture of the global CRO you're applying to. Understanding their values and work environment can help you tailor your responses during interviews, showing that you are a good 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 multi-therapeutic area work. Be ready to share specific examples of site visits you've conducted and how you handled challenges during those visits.
✨Emphasise Communication Skills
Since building strong site relationships is key, be prepared to discuss how you communicate effectively with site staff. Share examples of how you've resolved issues or improved site performance through your communication.
✨Demonstrate Problem-Solving Abilities
Prepare to discuss instances where you've identified and resolved site or protocol-related issues. Highlight your analytical skills and how you approach problem-solving, as this is crucial for the role.
