Medical Writer | Clinical Scientist | CER Writer
If you want a position where you're not lost in a 10 layer org chart for progression and you are surrounded by experienced people to learn and advance in your career. This is it.
Working with a well recognised Medical Device manufacturer as a Clinical Scientist, you are here to make sure the science holds up, the data says what it needs to say and that patients are genuinely better off for using the medical devices this company bring to market.
You’ll join a small but experienced Clinical Affairs team supporting highly regulated Class II & III devices, working to review all clinical and technical documentation to close out clinical gaps so the products remain safe and compliant.
If you’ve written or contributed to Clinical Evaluation Reports (CERs), understand EU MDR expectations, this could be the step you’ve been looking for.
Your core focus will be writing and maintaining Clinical Evaluation Reports (CERs) using real world data and clinical feedback.
You’ll:
- Analyse post-market data (e.g., complaints, feedback, literature, internal reports)
- Summarise performance and safety outcomes against MDR criteria
- Identify clinical data gaps and support study planning
- Contribute to risk assessments alongside R&D and Regulatory Affairs
- Attend relevant conferences and learn from clinical users directly
Must-haves:
- 1–2 years in the medical device industry
- Practical experience writing or contributing to CERs
- Strong analytical and written communication skills
- Comfort working with data and basic statistical tools (e.g., Excel, SPSS, R)
The company offer flexible working (2 days remote) and half day Fridays.
Not only that, they want to create opportunities for their staff to progress.
The last person hired here went from grad to senior specialist within 3 years.
If this sounds of interest, then please apply and I will be in touch.
