Medical Science Liaison, Spain

Location(s): Madrid Spain

Level of position: Senior Manager

Position type: Field

Reporting Line: Country Medical Affairs Director

How will your role help us transform hope into reality

The Medical Science Liaison (MSL) is a field-based scientific and clinical expert who strategically supports the medical objectives of Blueprint Medicines development programs. The MSL is responsible for identifying developing and managing peer-to-peer relationships with a variety of healthcare providers including hematologists oncologists pathologists dermatologists gastroenterologists and allergists/immunologists as well as basic scientists in academic and community hospitals.

The MSL will be accountable to engage in high quality scientific exchange about the science and clinical application of our precision medicine portfolio to variety of external stakeholders as well as obtain important insights about current practice treatment landscapes and emerging clinical and scientific addition the MSL is expected to build strong cross-functional relationships as well as provide meaningful subject-matter expertise to colleagues in Medical Affairs Clinical Research R&D Patient Advocacy and Commercial while maintaining full compliance with all relevant company industry legal and regulatory requirements. This position reports to the Country Medical Affairs Director.

What will you do

• Identify key opinion leaders and cultivate a network of experts for disease areas of focus
• Respond to unsolicited requests and engage in meaningful peer-to-peer scientific exchange of complex medical and scientific information with the oncology hematology pathology and rare disease community
• Provide internal stakeholders with feedback and insights from interactions and discussions with HCPs.
• Accurately profile country and define local dynamics related to patient diagnosis and referral for treatment
• Deliver medical/scientific presentations to internal & external stakeholders
• Assist with company-sponsored clinical trials and facilitation of investigator-initiated trials (ISTs)
• Lead planning and execution of regional advisory boards
• Collaborate with cross functional partners on internal projects and external initiatives
• Provide educational meeting support at scientific congresses
• Support training of cross functional teams
• Adhere to corporate and healthcare compliance guidance in all activities including those related to clinical trials scientific interactions with internal and external groups and responses to unsolicited requests for medical/scientific information
• Foster and maintain Blueprints positive and innovative culture
• Significant travel is required as part of this position

What minimum qualifications do we require

• Advanced Clinical/Science degree or professional credentials required (PhD MD/DO PharmD MSc)
• 3 years of experience in the biotech or pharmaceutical industry in Medical Affairs

What additional qualifications will make you a stronger candidate

• 3 years of experience in the biotech or pharmaceutical industry in Medical Affairs with experience working with cross-functional in-house and field-based teams
• Rare Disease and/or oncology/hematology experience strongly preferred; combined is ideal
• Immunology/allergy or dermatology experience of advantage
• Strong interpersonal presentation and communication skills and demonstrated ability to work collaboratively in a dynamic team-oriented environment
• Fluent written and spoken communication skills in English and in local language of geographic location where the position is based
• Creative problem-solving skills
• Positive solutions-oriented mindset
• Demonstrated self-starter and team player with strong interpersonal skills
• Adept nimble energetic and comfortable in a fast-paced dynamic and collaborative environment
• Capable of taking a hands-on approach and willing to roll up ones sleeves.
• Ensure compliance with corporate rules and local regulations
• Strong analytical skills especially with regard to understanding and interpreting scientific and clinical research and literature are essential
• 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

BlueprintMedicines 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 successleveraging 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 visitand follow us onX(formerly Twitter; @BlueprintMeds) andLinkedIn.

*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.

#LI-DNI