At a Glance
- Tasks: Conduct site monitoring visits and ensure data integrity and patient safety.
- Company: Globally recognised Functional Service Provider with a focus on quality over volume.
- Benefits: Flexible employment options, structured training, and career development opportunities.
- Other info: Home-based role with regional travel and a supportive work environment.
- Why this job: Join a dedicated team and make a real impact in clinical research.
- Qualifications: Experience in independent monitoring and a life sciences degree required.
The predicted salary is between 30000 - 40000 £ per year.
Location: United Kingdom (Home-based with regional travel)
Employment Type: Full-time, Permanent or part time considered (0.8 FTE)
About the Opportunity
We are currently partnering with a globally recognised Functional Service Provider to recruit six Clinical Research Associates across both CRA I and CRA II levels. Unlike traditional CRO models that often demand high-volume metrics, this FSP prioritises a qualitative approach to site management. You will be fully embedded into one of three dedicated single-sponsor teams, allowing you to focus deeply on a specific pipeline rather than juggling conflicting priorities across multiple thin accounts.
Why This Model is Different
- Quality Over Volume: The operational framework is designed to prevent burnout. Focus is placed on thorough, high-quality site relationships and meticulous data oversight rather than hitting a high volume of rushed visits.
- Dedicated Single-Sponsor Teams: You will work exclusively within one sponsor pipeline. This provides the stability and integration of working directly for a major pharmaceutical partner, backed by the infrastructure and career development of a top-tier FSP.
- Leading Site Approach: You will be trusted to manage your sites autonomously, acting as the primary point of contact and driving engagement through a collaborative, solutions-oriented approach.
- Structured Training: For CRA I candidates making their first career step, or CRA IIs looking to solidify their expertise, the onboarding and continuous professional development programmes are highly structured and tailored to your experience level.
Key Responsibilities
- Conduct the full cycle of site monitoring visits (qualification, initiation, routine monitoring, and close-out) in accordance with ICH-GCP guidelines, sponsor SOPs, and UK regulatory requirements.
- Manage site performance, ensuring data integrity, patient safety, and protocol compliance.
- Act as the main bridge between the sponsor and the investigative sites, resolving complex queries efficiently.
- Maintain accurate and timely trip reports and follow-up correspondence within required timelines.
What We Are Looking For
- For CRA I: A minimum of 6 months of independent, hands-on monitoring experience within the UK (including on-site or robust remote monitoring of data and regulatory binders).
- For CRA II: Between 12 to 18 months of independent UK monitoring experience, demonstrating strong site management skills and the ability to troubleshoot complex study issues.
- A life sciences degree (or equivalent nursing/medical qualification).
- Thorough working knowledge of ICH-GCP guidelines and UK clinical trial regulations.
- A valid UK driving licence and the willingness to travel to sites regionally.
To Apply
If you are looking for an environment that values clinical quality and offers a clear, sustainable path for career progression, please apply with your CV today. All applications will be handled with strict confidentiality.
FSP CRA I or CRA II in England employer: CCS-Global
Join a leading Functional Service Provider that prioritises quality over volume, offering a supportive work culture where you can thrive as a Clinical Research Associate. With dedicated single-sponsor teams, you'll enjoy the stability of focusing on a specific pipeline while benefiting from structured training and professional development tailored to your experience level. This home-based role with regional travel allows for a balanced work-life dynamic, making it an excellent choice for those seeking meaningful and rewarding employment in the clinical research field.
StudySmarter Expert Advice🤫
We think this is how you could land FSP CRA I or CRA II in England
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, attend industry events, and join relevant online groups. You never know who might have the inside scoop on a CRA position or can refer you directly.
✨Tip Number 2
Prepare for interviews by practising common CRA questions and scenarios. Think about your past experiences and how they relate to the role. We recommend doing mock interviews with friends or mentors to boost your confidence.
✨Tip Number 3
Showcase your passion for quality over quantity in your discussions. Highlight your commitment to thorough site management and patient safety, as this aligns perfectly with the FSP model we’re promoting.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re serious about joining our dedicated single-sponsor teams.
We think you need these skills to ace FSP CRA I or CRA II in England
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the specific skills and experiences that match the CRA I or CRA II roles. Highlight your monitoring experience and any relevant qualifications to show us you're the right fit!
Showcase Your Experience:When writing your application, emphasise your independent monitoring experience. We want to see how you've managed sites and ensured data integrity, so don’t hold back on those details!
Be Clear and Concise:Keep your application straightforward and to the point. Use clear language and avoid jargon where possible. We appreciate a well-structured application that’s easy for us to read.
Apply Through Our Website:For the best chance of success, make sure to apply directly through our website. This way, we can easily track your application and get back to you quicker!
How to prepare for a job interview at CCS-Global
✨Know Your Stuff
Make sure you brush up on your ICH-GCP guidelines and UK clinical trial regulations. Being able to discuss these confidently will show that you're serious about the role and understand the importance of compliance in clinical research.
✨Showcase Your Experience
Whether you're applying for CRA I or CRA II, be ready to talk about your independent monitoring experience. Prepare specific examples of how you've managed sites, resolved issues, and ensured data integrity. This will help demonstrate your capability and fit for the role.
✨Emphasise Quality Over Quantity
Since this FSP values a qualitative approach, highlight your commitment to building strong site relationships and delivering meticulous oversight. Share instances where you prioritised quality in your work, as this aligns perfectly with their operational framework.
✨Ask Insightful Questions
Prepare thoughtful questions about the team structure and training opportunities. This shows your interest in the role and helps you gauge if the company’s values align with yours. Plus, it gives you a chance to learn more about how they support career development.
