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🍊Our mission 

All new medicines need to undergo clinical trials to show they’re safe and effective. But today’s clinical trial infrastructure is stuck in the past, and the cost of developing new medicines has skyrocketed as a result. Patients have to wait longer and pay more for new treatments. 

Our mission is to fix this; we use software to help innovative companies run faster, more reliable, and patient-friendly clinical trials. We’re still a young company, but we’ve already had a big impact. Since founding the company in March 2021 we’ve helped run over 100 clinical trials involving tens of thousands of patients, with a customer NPS of 100.

We recently raised a $55m Series B round from Balderton Capital, with support from Creandum, Firstminute, Seedcamp, and Visionaries. 

🍊About the role


We’re looking for a CRA to ensure effective risk-proportionate monitoring of Lindus Health’s global portfolio of clinical trials. This covers both central and onsite monitoring, where site monitoring may be remote or may involve travelling to sites across the UK, to conduct in-person visits. You will undertake the preparation, conduct and then create reports for the trial monitoring visits. Central monitoring involves reviewing in real-time, accumulating trial data via our in-house platform, Citrus. This role is integral to maintaining high monitoring standards as our customer base grows significantly over the coming years and is our first full-time CRA hire in the UK.


You’ll work closely with our Clinical Operations, Product and Commercial teams, as well as the sponsor-side teams that make up our customer base.

🍊About you


We’d like to hear from you if…

  • You have 3+ years of work experience and meaningful time spent in a clinical trial monitoring role, including monitoring at NHS sites.

  • You understand how to take a risk-proportionate approach to monitoring and have been involved in developing monitoring plans to reflect this approach

  • You have a strong awareness of clinical trial regulations and are plugged in to potential changes to the regulatory environment.

  • You have great attention to detail and are a confident communicator with internal and external stakeholders

  • You have a bias to action - we're looking for someone who is proactive, organised and creative.

  • If you’ve already worked in a startup or early-stage environment this will be advantageous.

  • You’re comfortable travelling to conduct site visits across the UK (up to 60%)

  • Have a full UK driving licence

  • Previous involvement in central monitoring would be a bonus!

  • Previous involvement in US trials would be a bonus!

You belong here! If your experience and interests match with some of the above, we want you to apply.


🍊What you’ll focus on

  • Focus area 1: You’ll act as primary contact between Lindus Health and recruiting sites (as and when required), to lead effective monitoring according to trial protocols, including writing Monitoring Plans, arranging and conducting site monitoring visits and monitoring reports.

  • Focus area 2: You’ll coordinate and lead monitoring activities and deliverables on a company level, identifying and managing issues while proactively advising on improvements to our processes.

  • Focus area 3: You’ll work closely with our tech and product teams to help design best-in-class trial monitoring technology that exceeds customer demands

🍊What we offer

Make an impact across all areas of our business and fix one of the world’s most broken industries.

  • Competitive salary, plus meaningful stock options

  • Flexible working: We have an incredible office near London Bridge and encourage people to work 3 days per week from the office

  • Unlimited holidays; everyone is encouraged to take off at least 28 days each year

  • £60 monthly wellness allowance, which you can spend on our company health insurance scheme through AXA, a wellhub membership, or wellness activities and expenses of your choice!  

  • Enhanced Parental Leave: 16 weeks full pay for primary caregiver and 6 weeks full pay for secondary caregiver

  • £1,000 Learning and Development allowance each year to put towards courses, certifications, and development

  • Regular whole company and team events, both in person and virtually. 

  • Access to gym and retail discounts through our benefits platform Happl

  • A well-stocked pantry and drinks fridge, Monday breakfast spread and catered team lunch on a Thursday for the UK office every week!

  • Cycle-to-work scheme and other salary sacrifice options available

  • Charity events and fundraising opportunities through our charity partnership with the Forward Trust

🍊Our hiring process 

  • Initial conversation with our Talent team (30 minutes) 

  • Second meeting with a Senior member of our ClinOps team (30 minutes)

  • Functional interview with one of our Associate Directors and Senior Trial Manager (45 minutes) 

  • Values interview with a Cofounder and VP Clin Ops (30 minutes)  

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Average salary estimate

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What You Should Know About CRA, Lindus Health

At Lindus Health, we are on the mission to modernize clinical trials by utilizing innovative software solutions that allow companies to conduct faster, more reliable, and patient-friendly trials. We're a dynamic start-up and are thrilled to announce we’re looking for a Clinical Research Associate (CRA) to join our team in the United Kingdom. In this role, you will play a vital part in overseeing a global portfolio of clinical trials, ensuring effective monitoring is maintained through both central and onsite methods. As our first full-time CRA hire in the UK, your work will significantly influence our growth as you prepare, conduct, and report on trial monitoring visits. A key part of your responsibilities will involve using our in-house platform, Citrus, to review real-time trial data, alongside traveling to various UK sites for in-person visits, up to 60% of your time. We value a proactive, detail-oriented person with a solid foundation in clinical trial regulations and monitoring, as you’ll work closely with our Clinical Operations, Product, and Commercial teams. If you're passionate about making an impact in the clinical trial landscape, we want to hear from you!

Frequently Asked Questions (FAQs) for CRA Role at Lindus Health
What are the main responsibilities of a Clinical Research Associate at Lindus Health?

As a Clinical Research Associate (CRA) at Lindus Health, your core responsibilities will include conducting effective monitoring of clinical trials, preparing and conducting site visits, and generating monitoring reports. You will lead the monitoring process according to trial protocols, develop monitoring plans, and coordinate activities across various teams to ensure compliance with regulatory standards.

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What qualifications do I need to become a CRA at Lindus Health?

To qualify for the Clinical Research Associate position at Lindus Health, you should have at least 3 years of experience in clinical trial monitoring, particularly at NHS sites. A solid understanding of clinical trial regulations, experience in developing monitoring plans, and excellent communication skills are essential. Familiarity with central monitoring and previous experience in US trials can be advantageous.

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Can I expect to travel as a CRA at Lindus Health?

Yes, as a CRA at Lindus Health, you can expect to travel across the UK to conduct site visits. Travel can account for up to 60% of your role, so it’s important to be comfortable with traveling regularly to meet the various monitoring requirements of our clinical trials.

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What does a typical day look like for a Clinical Research Associate at Lindus Health?

A typical day for a Clinical Research Associate at Lindus Health may include preparing for site visits, conducting monitoring activities, reviewing trial data on our Citrus platform, and generating reports. You will also collaborate with clinical operations, product teams, and interact with sponsor-side teams to solve issues and improve monitoring processes.

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What benefits can I expect as a CRA working at Lindus Health?

As a CRA at Lindus Health, you can anticipate a competitive salary with stock options, unlimited holiday, a wellness allowance, enhanced parental leave, a generous learning and development allowance, and opportunities for team-building events. Plus, enjoy the perks of a well-stocked pantry and access to gym and retail discounts.

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Common Interview Questions for CRA
Can you describe your experience with clinical trial monitoring?

In answering this question, it's important to highlight specific experiences you've had monitoring clinical trials, particularly the methodologies you used. Mention any regulatory compliance knowledge and how you've handled challenges in your previous roles as it shows your adaptability and solutions-oriented mindset.

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How do you approach developing a risk-proportionate monitoring plan?

You should explain the steps involved in risk assessment and how it translates into your monitoring plan. Discuss your understanding of the trial protocols, potential risks identified, and how you prioritize monitoring activities based on those risks.

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What tools or platforms have you used for central monitoring?

Diving into your experience with specific tools, express your familiarity with monitoring systems. If applicable, mention how tools like electronic data capture (EDC) systems helped streamline your monitoring processes, showing your technical proficiency.

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Describe a time when you had to deal with a significant issue during a trial.

Provide a specific example where you encountered an issue and detail your approach to resolving it. Focus on the outcome and what you learned from the experience, demonstrating your problem-solving abilities.

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What strategies do you use to maintain strong communication with trial sites?

Discuss various communication techniques you've employed, such as regular updates, in-person visits, or feedback mechanisms. Highlight your proactive approach to ensuring all site staff are on the same page regarding trial protocols.

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Have you worked in a start-up or early-stage environment before? If so, how did that experience shape you?

If applicable, share your experiences from the startup environment, emphasizing how it has made you more agile, creative, and adaptable. Discuss how the fast-paced nature of such environments has prepared you for the role at Lindus Health.

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What do you think is the most critical aspect of monitoring clinical trials?

In your answer, consider discussing regulatory compliance, patient safety, data integrity, or relationship management. Justify your choice with a brief explanation and link it back to how it will impact trials positively.

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How do you stay informed about changes in clinical trial regulations?

Convey your commitment to staying updated through various methods, such as attending training sessions, subscribing to relevant journals, or being part of professional networks. This shows your dedication to continuous learning in the CRA role.

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What role does teamwork play in your work as a CRA?

Emphasize the importance of collaboration in a CRA role, including working with various departments or stakeholders in the trial process. Share examples of how teamwork has led to successful trials or resolved challenges effectively.

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Why do you want to work as a CRA at Lindus Health?

Relate your personal career goals to the mission and culture at Lindus Health. Express your enthusiasm for contributing to innovative solutions in clinical trials and your alignment with the company's goals for improving patient outcomes.

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Clinical trials are in crisis. The industry hasn't changed in 30 years, and the cost of bringing new medicines to market is skyrocketing as a result. Lindus Health’s mission is to fix this.

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DATE POSTED
April 16, 2025

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