Director, Field Medical Affairs (Rare Diseases)

Regeneron Pharmaceuticals, Inc; Madrid; Híbrido; EUR 100.000 - 150.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical company is seeking a Medical Director, Field Medical Affairs for Rare Diseases in Madrid, Spain. This hybrid role requires an advanced clinical or scientific degree and over 12 years of experience in related fields. Responsibilities include leading scientific discussions, evaluating market access strategies, and supporting clinical trials. Candidates should have a strong ability to build relationships and translate clinical data into actionable insights, with fluency in English required. Experience in rare disease therapies is advantageous.

Formación

• At least 12 years of experience in clinical practice, managed care, or the pharmaceutical industry.
• Minimum of two years in Medical Affairs.
• Experience launching rare disease therapies is a plus.

Responsabilidades

• Leading scientific discussions with healthcare professionals.
• Evaluating health technology assessments and reimbursement pathways.
• Collaborating across functions to support speaker training.
• Sharing field insights to inform medical planning.
• Supporting post-approval clinical trials.

Conocimientos

Strategic problem solving

Building trusted relationships

Fluency in English

Translating clinical data

Educación

Advanced clinical or scientific degree (MD, DO, PharmD, or PhD)

Descripción del empleo

We’re hiring a Medical Director, Field Medical Affairs (Rare Diseases) to help advance care in cardiovascular, muscle, and bone conditions. This hybrid role blends strategic medical planning with field-based scientific engagement across select European countries. You’ll join a collaborative international team focused on launching innovative therapies and strengthening partnerships that improve patient outcomes. If you’re motivated by scientific excellence and the opportunity to shape rare disease care, we’d love to hear from you.

A Typical Day:

• Leading scientific discussions with healthcare professionals and key opinion leaders.
• Evaluating health technology assessments, reimbursement pathways, and market access strategies.
• Responding to medical inquiries with accuracy and regulatory compliance.
• Collaborating across functions to support speaker training and promotional review.
• Sharing field insights to inform medical planning and product development.
• Supporting post-approval clinical trials from design to reporting.
• Partnering with CRO medical monitors and study teams to enhance site engagement.

This Role May Be For You If:

• You’re a strategic problem solver who thrives on connecting science with real‑world impact.
• You enjoy building trusted relationships and engaging in scientific dialogue.
• You’re comfortable navigating complexity and making informed decisions in dynamic environments.
• You take pride in translating clinical data into clear, actionable insights.
• You’re driven to advance rare disease innovation and improve patient outcomes.
• You’re adaptable and confident managing travel and engagement across diverse European healthcare systems.

To be considered, you’ll need an advanced clinical or scientific degree (MD, DO, PharmD, or PhD) and at least 12 years of experience in clinical practice, managed care, or the pharmaceutical industry, including a minimum of two years in Medical Affairs. Experience as a Medical Science Liaison or in a similar role is a plus. You must reside within the designated territory and be able to travel up to 50%. Fluency in English is required. We encourage candidates with experience launching rare disease therapies, contributing to clinical trial design, and proficiency in French, Spanish, Italian, or German.