Clinical Scientist in Sheffield

Energy Jobline ZR; Sheffield; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

A leading medical device company in Sheffield is seeking an experienced Clinical Scientist to write and maintain Clinical Evaluation Reports (CERs). This role offers flexible working options, including 2 days remote, and encourages career progression. Candidates should have 1–2 years in the medical device industry and be comfortable working with data and statistical tools. Apply now for a chance to work with a dedicated Clinical Affairs team.

Benefits

Flexible working (2 days remote)

Half-day Fridays

Qualifications

• 1–2 years in the medical device industry.
• Practical experience writing or contributing to Clinical Evaluation Reports (CERs).

Responsibilities

• 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.

Skills

Strong analytical and written communication skills

Comfort working with data and basic statistical tools

Tools

Excel

SPSS

R

Job description

Energy Jobline is the largest and fastest growing global Energy Job Board and Energy Hub. We have an audience reach of over 7 million energy professionals, 400,000+ monthly advertised global energy and engineering jobs, and work with the leading energy companies worldwide.

We focus on the Oil & Gas, Renewables, Engineering, Power, and Nuclear markets as well as emerging technologies in EV, Battery, and Fusion. We are committed to ensuring that we offer the most exciting career opportunities from around the world for our jobseekers.

Job Description

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 offers 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.