Clinical Quality & Trials Coordinator in London
Clinical Quality & Trials Coordinator

Clinical Quality & Trials Coordinator in London

London Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Support clinical trials and manage essential administrative tasks in a dynamic team.
  • Company: Leading lifescience company based in London with a focus on innovation.
  • Benefits: Full-time position with opportunities for professional growth and development.
  • Why this job: Join a passionate team and contribute to groundbreaking clinical research.
  • Qualifications: Bachelor's degree and 2 years of experience in life sciences required.
  • Other info: Office-based role with a collaborative and supportive work environment.

The predicted salary is between 36000 - 60000 £ per year.

A lifescience company in London is seeking a Clinical Affairs Assistant to support the clinical team in managing clinical trials and performing various administrative tasks.

The ideal candidate should have a Bachelor's degree and a minimum of 2 years of experience in the life science field. Proficiency in English and Microsoft Office is essential.

This is an office-based, full-time position with responsibilities including document management and regulatory support.

Clinical Quality & Trials Coordinator in London employer: Meditrial

Join a leading lifescience company in London that values innovation and collaboration, offering a dynamic work culture where your contributions directly impact clinical trials and patient outcomes. With a strong emphasis on employee development, you will have access to ongoing training and growth opportunities, alongside a supportive team environment that fosters creativity and excellence in the life sciences field.
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Contact Detail:

Meditrial Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Quality & Trials Coordinator in London

✨Tip Number 1

Network like a pro! Reach out to professionals in the life science field on LinkedIn or at industry events. We can’t stress enough how personal connections can open doors for you.

✨Tip Number 2

Prepare for interviews by researching the company and its clinical trials. We want you to show genuine interest and knowledge about their work, which will definitely impress the hiring team.

✨Tip Number 3

Practice your responses to common interview questions. We recommend using the STAR method (Situation, Task, Action, Result) to structure your answers, especially when discussing your experience in document management and regulatory support.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take that extra step to connect with us directly.

We think you need these skills to ace Clinical Quality & Trials Coordinator in London

Bachelor's Degree
Clinical Trials Management
Administrative Skills
Document Management
Regulatory Support
Proficiency in English
Microsoft Office
Life Science Knowledge
Attention to Detail
Communication Skills
Organisational Skills
Team Collaboration

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your relevant experience in the life science field. We want to see how your background aligns with the role of Clinical Quality & Trials Coordinator, so don’t be shy about showcasing your skills!

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 previous roles have prepared you for this position. We love seeing enthusiasm and a personal touch!

Showcase Your Skills: Since proficiency in Microsoft Office is essential, make sure to mention any specific tools or projects where you've used these skills effectively. We appreciate candidates who can demonstrate their technical abilities clearly.

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, it’s super easy to do!

How to prepare for a job interview at Meditrial

✨Know Your Stuff

Make sure you brush up on your knowledge of clinical trials and the life sciences sector. Familiarise yourself with common terminologies and processes, as well as any recent developments in the field. This will show that you're not just qualified but genuinely interested in the role.

✨Showcase Your Experience

Prepare to discuss your previous roles and how they relate to the responsibilities of a Clinical Quality & Trials Coordinator. Highlight specific examples where you've managed documents or supported regulatory processes, as this will demonstrate your hands-on experience and problem-solving skills.

✨Master Microsoft Office

Since proficiency in Microsoft Office is essential, make sure you're comfortable with all its features, especially Excel for data management and Word for documentation. Consider preparing a few examples of how you've used these tools effectively in past roles to streamline processes.

✨Ask Insightful Questions

Prepare thoughtful questions about the company's clinical trials and their approach to quality assurance. This not only shows your enthusiasm for the position but also helps you gauge if the company aligns with your career goals. It’s a great way to engage with the interviewers and leave a lasting impression.

Clinical Quality & Trials Coordinator in London
Meditrial
Location: London
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  • Clinical Quality & Trials Coordinator in London

    London
    Full-Time
    36000 - 60000 £ / year (est.)
  • M

    Meditrial

    50-100
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