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- Tasks: Support clinical trials and assist with quality management in the lifescience industry.
- Company: Join Meditrial UK Ltd, a leader in Pharma and Digital Health.
- Benefits: Confidential benefits discussed during dedicated meetings.
- Why this job: Make a real impact in healthcare while developing your skills.
- Qualifications: Bachelor’s degree and 2 years experience in life sciences required.
- Other info: Dynamic office environment with opportunities for growth.
The predicted salary is between 36000 - 60000 £ per year.
Industry: Lifescience Industry: Pharma, Medtech, Digital Health
Employment Type: Full-time
Job Functions: Clinical Affairs
Location: Meditrial UK Ltd. London, United Kingdom
Workplace: Office based
Benefits: Discussed confidentially during dedicated meeting
To learn more:
- Assist Clinical Quality Manager with various administrative tasks
- Support the clinical team for the management of clinical trials including the EDC System and CTMS as defined by the Quality System Procedures (SOPs)
- Support the clinical project team in assessment and management of clinical trials with medical devices (mainly cardiovascular therapeutic area) according to current regulations
- Collect, review, draft and track regulatory and investigator documents as required for the submission to the Competent Authorities and Ethics Committee; maintaining, updating and filing documents
- Perform administrative tasks required during study start-up activities (e.g. word processing, collecting study documents, relation management with Study Investigators, updating internal progress reports)
- SAE Notification to Competent Authorities and Ethics Committee
- Provide support for creation and maintenance of reports, charts, spreadsheets, documents and presentations
- Establish, maintain and update files and records as needed
Skills & Qualifications
- Education: Bachelor’s degree, Master is a plus
- Minimum 2 years experience in life science field and Quality Management
- Languages: proficiency in oral and written English (a second language would be a plus)
- Proficient in Microsoft Office (MS Outlook, MS Word, MS Excel, Ms Power Point)
Position: Clinical Quality Associate in London employer: Meditrial
Contact Detail:
Meditrial Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Position: Clinical Quality Associate in London
✨Tip Number 1
Network like a pro! Reach out to people in the lifescience industry, especially those working in clinical affairs. A friendly chat can open doors and give you insights that job descriptions just can't.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of clinical trials and quality management. We recommend creating a list of common interview questions and practising your answers with a mate. Confidence is key!
✨Tip Number 3
Showcase your skills! Bring along examples of reports, charts, or presentations you've created in the past. This will demonstrate your proficiency in Microsoft Office and your ability to manage clinical trial documentation effectively.
✨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 are proactive about their job search.
We think you need these skills to ace Position: Clinical Quality Associate in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Quality Associate role. Highlight your experience in clinical trials and quality management, and don’t forget to mention any relevant skills like proficiency in Microsoft Office.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about the life sciences industry and how your background makes you a perfect fit for the role. Keep it concise but impactful!
Showcase Relevant Experience: When filling out your application, be sure to showcase any specific experiences related to managing clinical trials or working with regulatory documents. This will help us see how you can contribute to our team right away.
Apply Through Our Website: We encourage you to apply through our website for a smoother process. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at Meditrial
✨Know Your Stuff
Make sure you brush up on the specifics of clinical trials and quality management in the life sciences sector. Familiarise yourself with the EDC System and CTMS, as well as current regulations related to medical devices, especially in the cardiovascular area.
✨Showcase Your Experience
Prepare to discuss your previous roles and how they relate to the responsibilities of a Clinical Quality Associate. Highlight any experience you have with regulatory documents, administrative tasks, or managing clinical trials, as this will demonstrate your capability for the role.
✨Be Ready for Scenario Questions
Expect questions that assess your problem-solving skills in real-world situations. Think about past challenges you've faced in clinical settings and how you overcame them. This will show your ability to handle the demands of the job.
✨Practice Your Communication Skills
Since proficiency in English is crucial, practice articulating your thoughts clearly and confidently. You might also want to prepare for questions about how you would communicate with study investigators and other stakeholders, as effective communication is key in this role.
