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For Companies At a Glance
- Tasks: Conduct site visits and monitor clinical research projects across the UK.
- Company: Join a leading global CRO trusted by top pharmaceutical companies.
- Benefits: Enjoy flexible home-based working and a competitive salary with great perks.
- Why this job: Make a real impact on global health while enjoying a balanced travel schedule.
- Qualifications: 18-24 months of 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.
(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, webinars, 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. Staying updated on these standards will not only enhance your knowledge but also demonstrate your commitment to compliance during interviews.
✨Tip Number 3
Prepare to discuss your independent monitoring experience in detail. Be ready to share specific examples of how you've handled site visits, resolved issues, and maintained relationships with sites, as this will showcase your expertise.
✨Tip Number 4
Highlight your multi-therapeutic area experience if applicable. If you've worked across various therapeutic areas, make sure to mention this during discussions, as it can set you apart from other candidates.
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 understanding of the role. Mention specific experiences that demonstrate your ability to conduct site visits and maintain compliance with regulations.
Highlight Key Skills: In your application, clearly outline your communication, organisational, and problem-solving skills. Provide examples of how you've successfully managed 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
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 visits effectively.
✨Emphasise Communication Skills
Since building strong relationships with sites is crucial, be ready to provide examples of how you've successfully communicated with site staff. Discuss any mentoring experiences you’ve had with junior CRAs to showcase your leadership abilities.
✨Prepare for Travel Discussions
Given the travel requirements of the role, be honest about your willingness to travel and share any relevant experiences. Discuss how you manage your time and maintain work-life balance while on the road.
