Medical Affairs Director

EPM Scientific; Antwerpen; Sur place; EUR 120 000 - 180 000; Plein temps

Résumé du poste

EPM Scientific is partnering with an international healthcare company focused on wound care, skin health, and medical technologies. They seek a Medical Affairs Director to lead global medical and clinical strategy across an expanding portfolio and pipeline.

The role entails defining evidence-generation roadmaps to support regulatory submissions, lifecycle management, market access, and commercial objectives; and providing strategic leadership for regulatory, quality, R&D, and cross-functional

Qualifications

• Advanced degree in a scientific/clinical field (MD, PharmD, PhD)
• 10+ years in Medical Affairs, Clinical Affairs, or related
• Experience in wound care, dermatology, skin health, or medical devices
• Deep expertise in clinical evidence generation, PMCF, and regulatory support
• Proven success leading cross-functional teams in international settings
• Experience supporting regulatory submissions and lifecycle management
• Strong ability to engage with KOLs, healthcare professionals and societies
• Commercial acumen to align medical strategy with business goals
• Previous people management and leadership experience
• Experience in growing SME or entrepreneurial healthcare environments is desirable

Responsabilités

• Lead global medical and clinical evidence generation strategy across products and pipeline.
• Define roadmaps to support regulatory submissions, lifecycle management and market access.
• Oversee clinical investigations, PMCF, and real-world evidence programs.
• Provide strategic medical guidance to Regulatory, Quality, R&D, Market Access and Commercial teams.
• Build and manage Medical Affairs and Clinical Affairs teams; ensure execution of programs.
• Engage with key opinion leaders and medical societies worldwide.
• Translate data into insights for product positioning and differentiation.
• Collaborate cross-functionally to support reimbursement and HEOR initiatives.

Connaissances

Cross-functional leadership

Stakeholder management

Strategic leadership

Clinical evidence generation

KOL engagement

Formation

MD/PhD/PharmD or equivalent

Description du poste

Medical Affairs Director (PR/607660) Flemish Region, Belgium

EPM Scientific are currently partnered with an international healthcare company focused on innovative wound care, skin health, and medical technologies. They are seeking a Medical Affairs Director to lead the global medical and clinical strategy across an expanding product portfolio and pipeline. This position will play a critical role in aligning clinical evidence generation, regulatory requirements, and commercial objectives to support continued international growth.

Role Overview

• Start Date: Flexible
• Location: Europe (Regular travel to Belgium HQ )
• Contract Type: Permanent, Full-Time

Key Responsibilities

• Develop and lead the global medical and clinical evidence generation strategy across marketed products and pipeline assets.
• Define clinical development and evidence-generation roadmaps to support regulatory submissions, lifecycle management, market access, and commercial objectives.
• Provide strategic oversight of clinical investigations, PMCF activities, real-world evidence programs, and broader clinical research initiatives.
• Act as the senior medical expert supporting Regulatory Affairs, Quality, R&D, Market Access, and Commercial teams.
• Lead and develop Medical Affairs and Clinical Affairs teams, ensuring successful execution of clinical programs and scientific engagement activities.
• Build relationships with key opinion leaders, scientific experts, medical societies, and external stakeholders globally.
• Translate clinical and scientific data into actionable insights that support product positioning, differentiation, and business growth.
• Partner cross-functionally to ensure evidence-generation plans support reimbursement, HEOR, and market access requirements.

Requirements

• Advanced scientific or clinical degree (MD, PharmD, PhD, or equivalent).
• 10+ years of experience in Medical Affairs, Clinical Affairs, Clinical Development, or Medical Strategy within medical devices, pharma, biotech, or healthcare.
• Strong experience in wound care, dermatology, skin health, medical devices, or related therapeutic areas.
• Deep expertise in clinical evidence generation, PMCF, clinical investigations, and regulatory support.
• Demonstrated success leading cross-functional teams within an international environment.
• Experience supporting regulatory submissions and product lifecycle management.
• Strong track record engaging with KOLs, healthcare professionals, medical societies, and external stakeholders.
• Commercial acumen with the ability to align medical and clinical strategy to business objectives.
• Previous people management and leadership experience.
• Experience within a growing SME or entrepreneurial healthcare environment is highly desirable.
• Excellent communication, stakeholder management, and strategic leadership skills.