Global Medical & Clinical Strategy Director

Marketing - Product Specialist (M/W); Belgique; Sur place; EUR 120 000 - 190 000; Plein temps

Résumé du poste

Flen Health is seeking a Medical & Clinical Affairs Director to shape global medical strategy, operations, and cross-functional market success. Based in Belgium-Kontich, this role reports to the CEO and defines the evidence roadmap for MDR lifecycle management and regulatory submissions.

You will align medical initiatives with commercial strategy, line-manage Clinical Project Managers, and lead international cross-functional teams to maximize patient impact and business growth.

Qualifications

• Advanced scientific or clinical degree (MD, PharmD, PhD, or equivalent) is required.
• 10+ years of progressive experience in Clinical Affairs, Medical Affairs, Clinical Development, or Medical Strategy within the medical device or healthcare industry.
• Experience in skin care, wound care, or closely adjacent therapeutic areas.
• Deep expertise in clinical evidence generation, PMCF design, and stringent MDR clinical compliance requirements.
• Demonstrated track record translating clinical evidence into commercially successful product positioning and measurable business impact.

Responsabilités

• Define, champion, and lead the comprehensive medical and clinical evidence strategy across Flen Health’s portfolio, with focus on Flaminal pipeline products and next-generation innovations.
• Provide senior clinical leadership across the global organization and oversee all clinical investigations and PMCF activities.
• Directly line-manage and mentor Clinical Project Managers, ensuring timely and compliant execution of trial protocols.
• Drive the scientific engagement strategy and medical education direction to support commercial growth and strategic partnerships.

Description du poste

Flen Health is seeking a Medical & Clinical Affairs Director to shape global medical strategy, operations, and cross-functional market success. Based in Belgium-Kontich, this role reports to the CEO and defines the evidence roadmap for MDR lifecycle management and regulatory submissions.

You will align medical initiatives with commercial strategy, line-manage Clinical Project Managers, and lead international cross-functional teams to maximize patient impact and business growth.