Director, Field Medical Affairs (Rare Diseases)

Regeneron Pharmaceuticals, Inc; Milano; Ibrido; EUR 90.000 - 130.000; Tempo pieno

Descrizione del lavoro

A biopharmaceutical company is seeking a Medical Director for Field Medical Affairs to advance care in rare diseases. This hybrid position involves strategic planning and scientific engagement across Europe. Candidates should have an advanced degree and extensive experience in clinical practice or the pharmaceutical industry. Responsibilities include leading scientific discussions, evaluating technology assessments, and supporting clinical trials. Fluency in English and abilities in other European languages are beneficial.

Competenze

• At least 12 years of experience in clinical practice, managed care, or pharmaceutical industry.
• Minimum of two years in Medical Affairs.
• Experience as a Medical Science Liaison or in a similar role is a plus.
• Fluency in French, Spanish, Italian, or German is encouraged.

Mansioni

• Lead scientific discussions with healthcare professionals.
• Evaluate health technology assessments and market access strategies.
• Respond to medical inquiries with accuracy.
• Collaborate to support speaker training.
• Share field insights for medical planning.
• Support post-approval clinical trials.
• Partner with CRO medical monitors.

Conoscenze

Strategic problem solving

Building relationships

Translating clinical data

Fluency in English

Experience in rare disease therapies

Navigating healthcare systems

Formazione

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

Descrizione del lavoro

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.