Medical Advisor, Italy

Location(s): Rome, Italy

Level of position: Associate Director

Position type: 65% Office-based, 35% Field-based (Or office-based with 30% business travel)

Reporting Line: The position reports to the Country Medical Lead

How will your role help us transform hope into reality?

The Medical Advisor role at Blueprint Medicines is a critical position within the organization, responsible for providing medical, scientific and strategic expertise to support Italy's development and commercialization programs. As a Medical Advisor, you will play a key role in driving the success of Blueprint's mission to improve and extend the lives of as many patients as possible through precision therapy. You will be a reliable bridge between clinical research, market access and commercialization and within the overall organization building strong relationships and collaboration with external and internal stakeholders.

As a Medical Advisor you will be living and sharing our core values and will be driven by the pursuit of new ideas, new innovations, and new ways of thinking to help advancing a diverse portfolio of innovative therapies for mast cell disorders, including systemic mastocytosis and chronic urticaria, and cancer.

What will you do?

• Proactively manage KOLs in the interest of Blueprint at the country level through your deep knowledge of the country's KOLs landscape.
• Establish and maintain strong relationships with KOLs, HCPs and PI's and be recognized by them as Blueprint's reference point and connector.
• Represent the company at relevant medical conferences and symposia.
• Foster the establishment and maintenance of local scientific advisory boards, round tables, expert meetings and scientific advocacy development.
• Closely cooperate with the country Medical Lead supporting the execution of medical plans as well as taking over the co-ordination of specific scientific projects.
• Cultivate a trustful and effective two-way collaboration with MSLs, supporting their presence in the field.
• Provide a source of key medical knowledge on the company's products and ensure that all regulatory requirements are met and aligned with local and Global standards.
• Maximize your skills in critically analyzing and interpreting clinical trial data, real-world evidence, and scientific literature. You will communicate the clinical implications of data and contribute to the development of scientific publications and presentations.
• Collaborate in insights collection and analysis to be translated into guidance for internal colleagues from different functions across the company.
• Leverage your expertise and excellence to contribute to the development and execution of the medical strategy.
• Build strong collaborative relationships with cross functional team to ensure alignment with medical and business objectives.
• Actively support upcoming launches by the means of Blueprint Medicines company sponsored symposia and other activities.
• Develop and deliver medical education programs for internal teams, healthcare professionals, and other stakeholders.
• Collaborate closely with International Medical teams to identify key data/material gaps and help in developing medical material and resources.
• Review product presentations and training materials, provide medical input into promotional campaigns and provide medical input in the health benefit discussion related to new products.
• Support interventional and non-Interventional clinical trials in close collaboration with Clinical development, Clinical Operations and Global Medical Affairs teams. Ensure a strategic approach to such programs, and the development of clinical data to support the appropriate use of the Company's products.
• Actively support the Medical Lead in developing and executing patient advocacy strategies, fostering meaningful partnerships with patient organizations and advocacy groups. Ensure that patient perspectives are integrated into medical plans, scientific communications, and strategic decision-making, in alignment with our patients first value.

What minimum qualifications do we require?

• Advanced Clinical/Science degree or professional credentials required (PhD, MD, PharmD, MSc).
• 5+ years of experience in the biotech or pharmaceutical industry in a similar role.

What additional qualifications will make you a stronger candidate?

• Excellent communication and presentation skills, with the ability to effectively communicate complex scientific concepts to diverse audiences.
• Familiarity with established and emerging regulatory frameworks (including AI, GDPR, EFPIA and Farmindustria) to ensure compliance and strategic alignment in medical activities.
• Demonstrable experience in the implementation of launches (pre- and post- launch plans).
• Solid understanding of the capabilities of the medical affairs function, the Hematology/Oncology/Allergy medical environment as well as Regulatory, HTA, Early Access Program and RCTs requirements.
• Seek input from the team to make key decisions while ensuring final decisions are taken quickly and effectively.
• Solid customer orientation; science-based, but good understanding of marketing needs; negotiation skills.
• Immunology/allergy and/or oncology/hematology experience preferred.
• Flexibility, with positive attitude, strong ability to multitask, prioritize projects effectively and communicate at all levels within the company.
• Ability to critically assess, adopt and integrate digital and innovative tools into medical affairs practice (RWE, PROs, digital biomarkers)
• Has confidence and optimism, enabling the development of strong relationships internally and externally with executive level leaders.
• Demonstrate respect for others by seeking to understand how they think about issues/opportunities; has an appreciation for others' strengths/development areas to increase overall collaboration and performance.
• Strong business acumen and courage of one's convicitons; however, stands by organizational decisions once made.
• High degree of emotional intelligence, always displaying candor and integrity, combined with the ability to manage complexity.
• Commitment to our Core Values: Patients First, Thoughtfulness, Urgency, Trust, Optimism

Why Blueprint?

At Blueprint Medicines, we achieve impactful results because of our global crew of compassionate innovators - the Blue Crew. Through authentic relationships and our collective entrepreneurial spirit and action, we are each empowered to take ownership and execute with strategic prioritization. We put trust in our people to break through norms and conventions using their individual strengths and insights, which drives our success.

This is the place where the extraordinary becomes reality, and you could be part of it.

Patients are waiting. Are you ready to make the leap?

Blueprint Medicines, a Sanofi company, is a global biopharmaceutical company that seeks to improve and extend patients' lives by solving important medical problems, with a focus on allergy/inflammation and oncology/hematology. Our approach begins by targeting the root causes of disease, using deep scientific knowledge in our core focus areas and drug discovery expertise across multiple therapeutic modalities. We have a track record of success, leveraging our established research, development, and commercial capability and infrastructure, we aim to significantly scale our impact by advancing a broad pipeline of programs ranging from early science to advanced clinical trials in mast cell diseases and solid tumors. For more information, visit www.BlueprintMedicines.com and follow us on X (formerly Twitter; @BlueprintMeds) and LinkedIn.

*Blueflex is our operating model which optimizes culture, productivity, & flexibility by maximizing the critical strengths of in-person work with the benefits of added flexibility. Blueflex allows for mix of in-office and remote work, enables flexibility to meet individual and business needs and makes effective use of our facilities and resources. It is a culture enhancer.

Client-provided location(s): Rome, Italy

Job ID: Blueprint_Medicine-4547639007

Employment Type: OTHER

Posted: 2025-09-05T19:14:36