Clinical Trials Monitor

Clinical Trials Monitor

Full-Time 30000 - 40000 £ / year (est.) Home office (partial)
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Queen Mary University of London

At a Glance

  • Tasks: Monitor clinical trials and ensure high-quality standards in research.
  • Company: Join a dynamic clinical trials unit at Queen Mary University.
  • Benefits: Competitive salary, generous leave, pension scheme, and flexible working options.
  • Other info: Embrace a diverse and inclusive workplace with excellent development opportunities.
  • Why this job: Make a real difference in healthcare by supporting innovative clinical studies.
  • Qualifications: Experience in monitoring research studies and strong report writing skills.

The predicted salary is between 30000 - 40000 £ per year.

We are looking for a Quality Assurance Monitor to join a dynamic clinical trials unit supporting high quality clinical trials in primary care, psychiatry, women's health, surgery and beyond. The Pragmatic Clinical Trials Unit (PCTU) is located in the Centre for Evaluation and Methods and linked with the Unit for Social and Community Psychiatry based in Newham.

You will work with the Quality Assurance team and the ChariotMS Trial Manager. You will be responsible for working alongside one other monitor in overseeing the unit's regulated studies, primarily the ChariotMS study.

Responsibilities
  • Support the Quality Assurance team in monitoring and oversight of regulated clinical studies.
  • Work alongside a fellow monitor to oversee the ChariotMS study and other unit studies.
  • Write detailed, clear monitoring reports and appropriately escalated findings.
  • Adhere to Good Clinical Practice, Data Protection guidelines and Clinical Trials regulations.
Qualifications & Experience
  • Experience monitoring research studies.
  • Proficient at writing detailed and clear monitoring reports.
  • Knowledge of Good Clinical Practice, Data Protection guidelines and Clinical Trials regulations.
  • Ability to raise findings appropriately and manage escalations.
Benefits

We offer competitive salaries, access to a generous pension scheme, 30 days leave per annum (pro-rata for part‑time/fixed‑term), a season ticket loan scheme and access to a comprehensive range of personal and professional development opportunities. Flexible working arrangements and campus facilities support work‑life balance.

Equal Opportunity & Diversity

Queen Mary's commitment to a diverse and inclusive community is embedded in our appointment processes. Reasonable adjustments will be made at each stage of the recruitment process for any candidate with a disability. We are open to considering applications from candidates wishing to work flexibly.

Clinical Trials Monitor employer: Queen Mary University of London

Join a forward-thinking clinical trials unit at Queen Mary, where we prioritise high-quality research and foster a supportive work environment. With competitive salaries, generous leave, and a strong commitment to professional development, our team thrives on collaboration and innovation in the heart of Newham. We embrace diversity and offer flexible working arrangements, making us an excellent employer for those seeking meaningful contributions in clinical research.
Queen Mary University of London

Contact Detail:

Queen Mary University of London Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Trials Monitor

✨Tip Number 1

Network like a pro! Reach out to professionals in the clinical trials field on LinkedIn or at industry events. A friendly chat can lead to opportunities that aren’t even advertised yet.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of Good Clinical Practice and Data Protection guidelines. We want you to shine, so practice answering common questions related to monitoring clinical studies.

✨Tip Number 3

Showcase your report-writing skills! Bring along examples of your detailed monitoring reports to interviews. This will demonstrate your proficiency and give you an edge over other candidates.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who are proactive about their job search.

We think you need these skills to ace Clinical Trials Monitor

Quality Assurance
Monitoring Research Studies
Writing Monitoring Reports
Good Clinical Practice (GCP)
Data Protection Guidelines
Clinical Trials Regulations
Escalation Management
Attention to Detail
Communication Skills
Team Collaboration
Regulated Studies Oversight

Some tips for your application 🫡

Tailor Your Application: Make sure to customise your CV and cover letter for the Clinical Trials Monitor role. Highlight your experience in monitoring research studies and your knowledge of Good Clinical Practice. We want to see how your skills match what we're looking for!

Be Clear and Concise: When writing your application, keep it straightforward and to the point. Use clear language to describe your experiences and achievements. We appreciate a well-structured application that makes it easy for us to see your qualifications.

Show Your Passion: Let your enthusiasm for clinical trials and quality assurance shine through in your application. Share why you're excited about this role and how you can contribute to our team. We love candidates who are genuinely interested in what we do!

Apply Through Our Website: Don't forget to submit your application through our official website! This ensures that your application gets to the right place and helps us keep track of all candidates. We can't wait to hear from you!

How to prepare for a job interview at Queen Mary University of London

✨Know Your Regulations

Make sure you brush up on Good Clinical Practice, Data Protection guidelines, and Clinical Trials regulations. Being able to discuss these topics confidently will show that you’re serious about the role and understand the importance of compliance in clinical trials.

✨Showcase Your Monitoring Experience

Prepare specific examples from your past experiences where you successfully monitored research studies. Highlight any challenges you faced and how you overcame them. This will demonstrate your practical knowledge and problem-solving skills.

✨Write Clear Reports

Since writing detailed monitoring reports is a key responsibility, practice summarising complex information clearly and concisely. Bring a sample report if possible, or be ready to discuss how you approach report writing during the interview.

✨Teamwork is Key

You’ll be working alongside another monitor, so emphasise your ability to collaborate effectively. Share examples of how you’ve worked in teams before, especially in high-pressure environments, to show you can support each other in overseeing studies.

Clinical Trials Monitor
Queen Mary University of London
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