Clinical Trials Coordinator & Documentation Specialist
Clinical Trials Coordinator & Documentation Specialist

Clinical Trials Coordinator & Documentation Specialist

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 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 encourages growth within the clinical research field. Join us to be part of a team that is dedicated to advancing healthcare while enjoying the unique advantages of working in one of the world's most vibrant cities.
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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

✨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 your knowledge of Good Clinical Practice (GCP) and the latest trends in clinical trials. We want you to shine when discussing your experience and how it relates to the role!

✨Tip Number 3

Showcase your IT skills! Be ready to demonstrate your proficiency in Word, Excel, and PowerPoint during interviews. We know these tools are essential for the role, so let’s make sure you’re confident using them.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. We’re excited to see your passion for clinical research and how you can contribute to our team.

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

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 hold back on 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 impactful!

Showcase Your IT Skills: Since IT proficiency is key for this role, make sure to mention your experience with Word, Excel, and PowerPoint. We love seeing examples of how you've used these tools in previous roles, so don’t be shy!

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 – just follow the prompts!

How to prepare for a job interview at Meiragtx

✨Know Your GCP

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

✨Showcase Your Documentation Skills

Prepare examples of how you've managed study documents or assisted in regulatory submissions in previous positions. Bring along any relevant documentation samples (if permitted) to demonstrate your organisational skills and attention to detail.

✨Familiarise Yourself with the Company

Research the biopharmaceutical firm thoroughly. Understand their recent projects, values, and culture. This knowledge will help you tailor your answers and show that you're genuinely interested in being part of their team.

✨Practice IT Proficiency

Since IT skills in Word, Excel, and PowerPoint are essential, be ready to discuss how you've used these tools in your previous roles. Consider preparing a quick presentation or report to showcase your proficiency if asked during the interview.

Clinical Trials Coordinator & Documentation Specialist
Meiragtx

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