IVD Senior Regional Scientific Liaison, Europe

IVD Senior Regional Scientific Liaison, Europe

Mindray

Remote

Your mission

As Senior Regional Scientific Liaison – Europe, you will lead scientific and clinical initiatives that strengthen Mindray’s credibility and market position in IVD.

You will act as a bridge between clinical science, commercial strategy, and global headquarters, ensuring our products are supported by robust, ethical, and high‑quality clinical evidence.

What you will do

Lead European clinical studies

• Identify and initiate multi-country clinical study opportunities in collaboration with HQ Scientific Affairs and local Marketing teams
• Oversee study agreements, timelines, and deliverables
• Ensure full compliance with European regulatory and ethical requirements

Build and nurture KOL partnerships

• Identify, engage, and develop Key Opinion Leaders across Europe
• Establish long‑term collaborations with university hospitals and research institutions
• Position Mindray as a credible scientific partner, not just a supplier

Drive publications and scientific storytelling

• Support and coordinate peer‑reviewed publications, abstracts, and congress presentations
• Translate clinical data into compelling, high‑quality scientific content
• Ensure scientific rigor and consistency across all outputs

Collaborate across borders and functions

• Work closely with HQ, EU Marketing, Product Specialists, and local teams
• Align scientific initiatives with broader business and growth objectives
• Negotiate and manage institutional agreements with confidence and professionalism

Ensure compliance and excellence

• Prepare and review study protocols, contracts, and ethical submissions
• Maintain high standards of documentation, governance, and transparency
• Provide regular reporting, insights, and recommendations to EU and HQ leadership

What you bring

• Minimum 10 years’ experience in Scientific Affairs, Clinical Research, or Medical Affairs within the IVD industry
• Strong hands‑on experience managing European clinical studies and ethical committee interactions
• Proven ability to engage and influence senior scientific and clinical stakeholders
• Experience in scientific writing and publication processes (journals, abstracts, congresses)
• Excellent project management skills, able to manage multiple studies across different countries
• Advanced degree in Life Sciences, Biomedical Engineering, or similar (PhD or MSc preferred)
• Fluency in English plus at least one additional European language
• Willingness to travel across Europe (approx. 40%)