Clinical Trials Coordinator & Documentation Specialist in London
Clinical Trials Coordinator & Documentation Specialist

Clinical Trials Coordinator & Documentation Specialist in London

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

  • Tasks: Coordinate clinical trials and manage essential documentation for groundbreaking research.
  • Company: Leading biopharmaceutical firm in Greater London with a focus on innovation.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Why this job: Join a dynamic team making a real difference in healthcare through clinical research.
  • Qualifications: University degree in health sciences and experience in clinical research or pharma.
  • Other info: Fast-paced environment with a commitment to Good Clinical Practice.

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

A leading biopharmaceutical firm in Greater London seeks a Clinical Trials Administrator (CTA) to coordinate the logistical aspects of clinical trials while ensuring adherence to Good Clinical Practice (GCP).

Responsibilities include:

  • Managing study documents
  • Assisting in regulatory submissions
  • Maintaining trial supplies

The ideal candidate has a university degree in health sciences and experience in clinical research or the pharmaceutical industry. IT proficiency in Word, Excel, and PowerPoint is essential.

Clinical Trials Coordinator & Documentation Specialist in London employer: Meiragtx

As a leading biopharmaceutical firm in Greater London, we pride ourselves on fostering a dynamic work culture that prioritises innovation and collaboration. Our employees benefit from comprehensive professional development opportunities, competitive remuneration, and a supportive environment that values work-life balance, making us an excellent employer for those seeking meaningful careers in clinical research.
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Contact Detail:

Meiragtx Recruiting Team

StudySmarter Expert Advice 🤫

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

✨Tip Number 1

Network like a pro! Reach out to professionals in the biopharmaceutical 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 brushing up on GCP guidelines and recent trends in clinical trials. We recommend practising common interview questions with a friend to boost your confidence.

✨Tip Number 3

Showcase your IT skills! Be ready to discuss how you've used Word, Excel, and PowerPoint in previous roles. We love seeing candidates who can demonstrate their tech-savviness.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. We’re always on the lookout for passionate individuals ready to make an impact.

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

Clinical Trials Coordination
Good Clinical Practice (GCP)
Regulatory Submissions
Document Management
Trial Supply Management
Health Sciences Knowledge
Clinical Research Experience
Pharmaceutical Industry Experience
IT Proficiency in Word
IT Proficiency in Excel
IT Proficiency in PowerPoint

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in clinical research and any relevant qualifications. We want to see how your background aligns with the role of Clinical 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 experience makes you the perfect fit for our team. Keep it concise but engaging – we love a good story!

Show Off Your IT Skills: Since IT proficiency is key for this role, make sure to mention your experience with Word, Excel, and PowerPoint. We’re looking for someone who can handle documentation and data management like a pro, so give us the details!

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 don’t miss out on any important updates. Plus, it shows you’re keen to join our team!

How to prepare for a job interview at Meiragtx

✨Know Your GCP Inside Out

Make sure you brush up on Good Clinical Practice (GCP) guidelines before the interview. Being able to discuss how you've applied these principles in past roles will show your understanding and commitment to quality in clinical trials.

✨Showcase Your Document Management Skills

Prepare examples of how you've managed study documents in previous positions. Highlight your attention to detail and organisational skills, as these are crucial for a Clinical Trials Coordinator.

✨Familiarise Yourself with Regulatory Submissions

Research the regulatory submission process relevant to clinical trials. Be ready to discuss any experience you have in this area, as it will demonstrate your capability to assist in submissions effectively.

✨Demonstrate IT Proficiency

Since IT skills in Word, Excel, and PowerPoint are essential, consider preparing a brief demonstration or example of how you've used these tools in your work. This will help you stand out as a tech-savvy candidate.

Clinical Trials Coordinator & Documentation Specialist in London
Meiragtx
Location: London

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