
Clinical Evaluation Specialist
Hover or tap a row for full statistics (EUR / month on this chart).
Salary analysis
Compared with the selected benchmark ("All roles in London, United Kingdom"), this listing's salary midpoint is about 30% lower. The offer still falls within the benchmark range (€3,847–€15,737). The listed pay band (€6,250–€7,500) is tighter than the benchmark, which suggests lower salary variability. This benchmark is based on 10 comparable listings.
| Market | Lower bound (25th percentile) | Median | Upper bound (75th percentile) |
|---|---|---|---|
| All roles in London, United Kingdom | €3,847/per month | €7,124/per month | €15,737/per month |
About the role As a Clinical Evaluation Specialist, you’ll assess clinical evidence, interpret research and regulatory guidance, and help customers bring safe devices and updates to market. You’ll use AI-assisted workflows to navigate evidence, compare claims and surface questions for deeper review. You'll experiment with improvements to your workflows as model capabilities improve and work with our product, engineering and applied machine learning teams to improve the tools you use. Responsibilities - Assess clinical evaluation plans and reports submitted by our customers - Screen and action regulatory insights from the latest research, standards and guidance - Work with our product, engineering, design and applied machine learning teams to build and improve our systems - Work with our market access team to expand Scarlet's responsibility to new jurisdictions and certifications - Create content to explain complex regulatory topics to customers and prospects - Provide regulatory insights to prospects and customers Required qualifications - A degree in clinical medicine, nursing, dentistry, epidemiology or public health - Minimum of two years’ experience with the assessment of clinical data for medical devices - Minimum of two years’ experience in patient care - Knowledge of the fundamental principles of the assessment of clinical data for medical devices and medical statistics - Practical experience in conducting or monitoring clinical investigations or trials, or assessing clinical data - Exceptional written and verbal communication skills Preferred qualifications - Experience developing, implementing or evaluating medical device software - Knowledge or training in the relevant standards and guidance used for clinical evaluation, such as ISO 14155 and MEDDEV 2-7/1 Rev.4 - Knowledge of different clinical research methodologies, including experience designing or contributing to the development of clinical trials Interview process Intro call with Kim — 20 mins Interview with Sandy — 45 mins Technical interview with Kim — 1 hour Culture and values interviews with James and Jamie — 2 × 30 mins Referencing and offer
Job Details
Education Level
BachelorRecruitment Process
- 1Intro call
- 2Interview rounds
- 3Technical interview
- 4Culture and values interviews
- 5Referencing and offer

| Location | Active listings |
|---|---|
| London, United Kingdom | 1 |
| Remote - Global | 1 |
| Remote - Europe | 1 |
| Remote - United States | 1 |
| Role type | Active listings |
|---|---|
| Lead Auditor | 1 |
| Software Engineer | 1 |
| Role level | Active listings |
|---|---|
| Executive | 1 |
| Mid-Level | 1 |
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