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- Tasks: Assist in managing clinical trials and support the clinical quality team.
- Company: Join Meditrial, a leader in the lifescience industry.
- Benefits: Confidential benefits discussed during a dedicated meeting.
- Why this job: Make a difference in healthcare by working with innovative medical devices.
- Qualifications: Bachelor’s degree and 2 years of experience in life sciences required.
- Other info: Dynamic office environment with opportunities for growth in clinical affairs.
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
Responsibilities:
- 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 employer: Meditrial
Contact Detail:
Meditrial Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Position: Clinical Quality Associate
✨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 lead to insider info about job openings that aren’t even advertised yet.
✨Tip Number 2
Prepare for interviews by researching Meditrial and their projects. Knowing their work with cardiovascular medical devices will show you’re genuinely interested and ready to contribute from day one.
✨Tip Number 3
Practice your responses to common interview questions, especially around quality management and clinical trials. We all know how important it is to demonstrate your experience and skills confidently!
✨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 take that extra step!
We think you need these skills to ace Position: Clinical Quality Associate
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 our team at Meditrial.
Showcase Relevant Experience: When filling out your application, be specific about your previous roles in clinical affairs. Mention any administrative tasks you've handled and how they relate to the responsibilities listed in the job description.
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 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. Familiarise yourself with the EDC System and CTMS, as well as the regulations surrounding medical devices, especially in the cardiovascular area. This will show that you're not just interested in the role but also knowledgeable about the industry.
✨Showcase Your Experience
Prepare to discuss your previous experience in the life sciences field. Think of specific examples where you've supported clinical teams or managed documentation. Highlight any administrative tasks you've handled that relate to study start-up activities, as this will demonstrate your hands-on experience.
✨Be Ready for Regulatory Talk
Since you'll be dealing with regulatory documents and submissions, be prepared to talk about your understanding of the submission process to Competent Authorities and Ethics Committees. Brush up on any relevant regulations and be ready to discuss how you've navigated these in past roles.
✨Master Microsoft Office
As proficiency in Microsoft Office is a must, make sure you're comfortable using Excel for data management and PowerPoint for presentations. You might even want to prepare a sample report or presentation to showcase your skills during the interview. This will give you an edge and show that you're ready to hit the ground running.
