Clinical Science Scientist – Technical Writing & Data Evaluation

About the role

Join a world‑leading diabetes‑care team as a Scientist in the Clinical Science Team. You will be responsible for high‑quality technical writing and rigorous evaluation of clinical data to support regulatory compliance and CE marking of medical devices.

Key responsibilities

• Gather and assess clinical evidence from scientific literature and post‑market sources for internal and competitor devices.
• Prepare clear, accurate technical reports and documentation that meet MDR/IVDR standards.
• Review and appraise clinical data to ensure regulatory compliance and strategic alignment.
• Present complex findings in engaging formats to support product success.

Required profile

• Higher education qualification in a technical or scientific discipline.
• Exceptional scientific writing skills with meticulous attention to detail.
• Ability to adapt to multiple changing priorities and tight deadlines.
• Industry experience within a regulated scientific environment is preferred.

Required skills

• High proficiency in Microsoft Office.
• Experience with Power BI or Power Automate (advantageous).

What we offer

• 12‑month fixed‑term contract with competitive hourly rate.
• Opportunity to work on impactful medical‑device projects in diabetes care.
• Supportive team environment that values professional growth and technical excellence.