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- Tasks: Coordinate and manage clinical trials, ensuring compliance and high-quality patient care.
- Company: Re:Cognition Health, a leader in clinical research with a focus on innovation.
- Benefits: Competitive salary, 25 days annual leave, private health insurance, and continuous professional development.
- Why this job: Join a dynamic team making a real difference in healthcare through clinical trials.
- Qualifications: Life sciences degree, 1+ year experience in clinical trials, and Microsoft Office proficiency.
- Other info: Exciting opportunities for career growth and access to unique employee benefits.
The predicted salary is between 34000 - 38000 £ per year.
The Clinical Trials Coordinator role involves the set up and delivery of all clinical trials according to RCH governance, operational, financial and developmental strategies and in compliance with Good Clinical Practice (GCP) principles. Responsibilities include:
- Accountable for ICH-GCP compliance across all assigned studies.
- Ensuring the highest levels of customer/patient care and clinical delivery are maintained at all times.
- Supporting the development of the business by working closely with clinicians and consultants to maximise business opportunities and recruit patients.
- Adhering to the organisation’s policies and SOPs and ensuring all members of the clinical trials team are trained and compliant.
- Performing accurate and timely administration, including the entry of patient records on all necessary databases and forms.
- Ensuring that all patient records are accurate, stored appropriately, and that all confidential information is retained in accordance with data protection requirements.
- Maintaining the Centre to the highest standards as expected by the organisation and ensuring all equipment is calibrated and maintained in line with best practice.
- Ensuring adequate stock within the Centre is ordered in a timely way and controlled.
- Seeking feedback from patients regarding their experience and recording these findings to support the ongoing development of the service.
- Completing necessary start-up activities, including assisting the Clinical Trials Start Up Specialist with the completion and submission of Non-NHS SSI forms to the relevant REC for new studies.
- Performing internal audits of working practices within the Centre to measure compliance against company SOPs and GCP.
Essential requirements:
- Life sciences degree or similar with minimum 2:1.
- At least 1-year experience within clinical trials research.
- Proficiency in the use of Microsoft Office packages (Word, Excel, PowerPoint).
- Experience with electronic data capture (EDC) systems.
- Previous experience as a Clinical Trials Coordinator in a similar field within the private health sector.
Desirable:
- Ideally experience with cognitive clinical trials.
Salary: £34,000 - £38,000
Benefits:
- Continuous professional development.
- 25 Days Annual Leave + Bank Holidays, increasing to 30.
- Private Health Insurance.
- Life insurance.
- Employee Assistance Program.
- Pension Scheme.
- Perkbox.
- Free Mortgage Advisor Scheme.
- Electric Vehicle Scheme.
The successful applicant will have access to all Re:Cognition Health’s benefits.
Clinical Trials Coordinator - London in City of Westminster employer: Re:cognition Health Clinics
Contact Detail:
Re:cognition Health Clinics Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trials Coordinator - London in City of Westminster
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical trials field, attend industry events, and join relevant online groups. You never know who might have the inside scoop on job openings or can refer you directly.
✨Tip Number 2
Prepare for interviews by researching the company and understanding their clinical trials. Be ready to discuss how your experience aligns with their needs, especially around GCP compliance and patient care. Show them you’re not just a fit on paper!
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a quick thank-you email reiterating your interest in the role. It keeps you fresh in their minds and shows your enthusiasm for the position.
✨Tip Number 4
Apply through our website for the best chance at landing that Clinical Trials Coordinator role. We love seeing applications directly from our site, and it helps us keep track of all the amazing talent out there!
We think you need these skills to ace Clinical Trials Coordinator - London in City of Westminster
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Trials Coordinator role. Highlight your relevant experience in clinical trials and any specific skills that match the job description, like ICH-GCP compliance or proficiency in EDC systems.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical trials and how your background makes you a perfect fit for our team. Don’t forget to mention your life sciences degree and any relevant experiences.
Showcase Your Attention to Detail: In this role, accuracy is key! Make sure your application is free from typos and errors. This shows us that you can maintain the high standards we expect in clinical delivery and patient care.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, you’ll get to see all the benefits we offer!
How to prepare for a job interview at Re:cognition Health Clinics
✨Know Your GCP Inside Out
Make sure you brush up on Good Clinical Practice (GCP) principles before the interview. Being able to discuss how you've applied these principles in your previous roles will show that you're not just familiar with them, but that you can implement them effectively.
✨Showcase Your Experience
Prepare specific examples from your past experience in clinical trials research. Highlight your role in managing operational aspects and how you ensured compliance with ICH-GCP. This will demonstrate your hands-on knowledge and ability to handle the responsibilities of the role.
✨Familiarise Yourself with the Company
Research the organisation and its clinical trials. Understanding their focus areas and recent studies will help you tailor your answers and show genuine interest. It’s a great way to connect your skills with their needs during the conversation.
✨Prepare Questions for Them
Think of insightful questions to ask at the end of the interview. Inquire about their current trials or how they measure patient feedback. This shows that you’re proactive and genuinely interested in contributing to their success.