Careers at Eclevar Medtech

Build the future of
Medtech innovation.

We are a globally distributed CRO dedicated exclusively to high-risk medical devices. Join an elite team of clinical architects shaping the EU MDR and global landscape.

MILO Tech Hub 99.9% System Uptime
Global Reach 4 Hubs London • Paris • Tokyo • Pune
Clinical Data 100% MDR/FDA Compliant
Remote-First Culture
High-Risk Medtech Only
SaaS Technology DNA
Eclevar Global Network

A connected infrastructure.

🇫🇷 Paris EU Regulatory
🇬🇧 London UKCA Corridor
🇯🇵 Tokyo PMDA Japan
🇮🇳 Pune MILO Tech Hub
The Eclevar Medtech DNA

Why join our organization.

🎯

100% High-Risk Medtech.
Zero pharma distraction.

We perform one task at the highest global standard: the management of Class IIb and Class III devices. Become an elite specialist in EU MDR, UKCA, and PMDA.

💻

Proprietary technology
development.

We developed the MILO EDC and MILO Health platforms. Our team works with the most modern clinical technology stack in the industry.

🌐

Professional
autonomy.

A true remote-first culture built on trust, asynchronous communication, and extreme accountability. Own your schedule.

Voices of Eclevar

Hear from the strategists driving our global programs.

★★★★★

"Every team member understands Medtech. Rapid decision-making and proprietary tools like MILO make my expertise truly valued."

SM

Senior Regulatory Writer

Paris, France
★★★★★

"Working on cardiovascular implants is rewarding. The remote-first culture gives me freedom to manage my visits efficiently."

LK

Clinical Research Associate

London, UK
★★★★★

"Building data architecture that supports life-saving devices alongside clinical experts is a rewarding technical challenge."

PR

Lead Data Architect

Pune, India

Do not see a perfect fit?

Eclevar Medtech is always seeking exceptional regulatory experts and clinical leaders. If you possess deep Medtech expertise, we want to hear from you.

Reforming Clinical Evaluation of Medical Devices in Europe