Global Careers at Eclevar MedTech | Remote-First MedTech CRO Jobs
Careers · Remote-First · High-Risk Devices Only

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 EU MDR and the global landscape.

4 hubs: London · Paris · Tokyo · Pune Remote-first Class IIb & III only
Eclevar MedTech team receiving the Platinum Award at the xShare and EUCROF Awards in Amsterdam Platinum Award 2026

Join a team recognised with the Platinum Award at xShare & EUCROF.

Top prize in the xShare x European CRO Federation "EHDS & Clinical Research" Open Call, awarded to Eclevar MedTech and its Milo Health platform, presented at the EUCROF 2026 conference in Amsterdam.

Co-funded by the European Union

Horizon Europe · Grant Agreement No. 101136734 · Amsterdam, 2 Feb 2026

99.9%MILO Tech Hub system uptime
4Global hubs: London, Paris, Tokyo, Pune
100%MDR / FDA compliant clinical data
RemoteRemote-first, asynchronous culture
Our organisational DNA

Why the best clinical minds choose Eclevar.

01

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.

02

Proprietary technology

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

03

Professional autonomy

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

Global footprint

Four hubs, one distributed team.

🇫🇷
ParisEU Regulatory
🇬🇧
LondonUKCA Corridor
🇯🇵
TokyoPMDA Japan
🇮🇳
PuneMILO Tech Hub
Open positions

Current opportunities.

To apply, email careers@eclevar.com with the role title in the subject line.

RoleLocationType
Senior Clinical Research Associate (CRA)Europe (remote)Full-timeApply ↗
Senior Medical Writer (CER / PMCF)Paris / EU remoteFull-timeApply ↗
Clinical Data Manager (MILO EDC)Pune, IndiaFull-timeApply ↗
From the team

What it is like to work here.

★★★★★

"Deep specialism, real ownership and a modern tech stack. Every project pushes the standard higher."

Senior Regulatory Writer · Paris

★★★★★

"Remote-first done properly, with trust and accountability. I work with high-risk devices only, which keeps the work sharp."

Clinical Research Associate · London

★★★★★

"Building the MILO platform means engineering and clinical science sit at the same table. Rare and energising."

Lead Data Architect · Pune

Spontaneous applications welcome

If you possess deep MedTech expertise, we want to hear from you.

No matching role above? Send an unsolicited application. We are always looking for exceptional clinical, regulatory and data talent.

Send your application
Explore Eclevar

Reforming Clinical Evaluation of Medical Devices in Europe