Medical Science Liaison Spain Contractor

Blueprint Medicines; Madrid; Híbrido; EUR 60.000 - 100.000; Jornada completa

Descripción de la vacante

Join a forward-thinking biopharmaceutical company as a Medical Science Liaison, where you'll leverage your expertise to support clinical development and commercial goals. This role involves building relationships with healthcare providers, engaging in scientific exchanges, and contributing to impactful clinical trials. With a focus on oncology and rare diseases, you'll collaborate with cross-functional teams to drive innovation and compliance. Embrace a culture that values trust and creativity, and be part of a mission to alleviate human suffering through groundbreaking medicines.

Formación

• 3 years of experience in the biotech or pharmaceutical industry in Medical Affairs.
• Fluent written and spoken communication skills in English and local language.

Responsabilidades

• Identify key opinion leaders and cultivate a network of experts.
• Engage in meaningful peer-to-peer scientific exchange.
• Deliver medical/scientific presentations to stakeholders.

Conocimientos

Presentation Skills

Time Management

Clinical Research

Communication skills

GCP

Infusion Experience

Managed Care

Hospice Care

Conflict Management

Clinical Trials

Research Experience

Home Care

Educación

Advanced Clinical / Science degree (PhD, MD/DO, PharmD, MSc)

Descripción del empleo

Position type : fieldbased temporary for 12months

Reporting Line : This position reports into the Director of International Medical Affairs

How will your role help us transform hope into reality

The Medical Science Liaison (MSL) is a fieldbased scientific and clinical expert who strategically supports the medical objectives of Blueprint Medicines clinical development programs and commercialized products. The MSL is responsible for identifying developing and managing peertopeer 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 highquality scientific exchange about the science and clinical application of our precision medicine portfolio to a variety of external stakeholders as well as obtain important insights about current practice treatment landscape and emerging clinical and scientific data. In addition the MSL is expected to build strong crossfunctional relationships as well as provide meaningful scientific expertise to colleagues in Medical Affairs Clinical Development 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.

This position is a 12month contract.

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 peertopeer 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 companysponsored clinical trials and facilitation of investigatorinitiated trials (ISTs)
• Lead planning and 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 crossfunctional inhouse and fieldbased 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 teamoriented environment
• Fluent written and spoken communication skills in English and in local language of geographic location where the position is based
• Creative problemsolving skills
• Positive solutionsoriented mindset
• Demonstrated selfstarter and team player with strong interpersonal skills
• Adept nimble energetic and comfortable in a fastpaced dynamic and collaborative environment
• Capable of taking a handson 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

Blueprint Medicines is a global fully integrated biopharmaceutical company that invents lifechanging medicines. We seek to alleviate human suffering by solving important medical problems in two core focus areas : 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 proven track record of success with two approved medicines including bringing our medicine to patients with systemic mastocytosis (SM) in the U.S. and Europe. Leveraging our established research development and commercial capability and infrastructure we now 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 including SM and chronic urticaria breast cancer and other solid tumors.

• Blueflex is our operating model which optimizes culture productivity & flexibility by maximizing the critical strengths of inperson work with the benefits of added flexibility. Blueflex allows for mix of inoffice 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.

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Required Experience :

Contract

Key Skills

Presentation Skills,Time Management,Clinical Research,Communication skills,GCP,Infusion Experience,Managed Care,Hospice Care,Conflict Management,Clinical Trials,Research Experience,Home Care