Medical Science Liaison

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company’s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com.

Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.

Brief Team/department Description

We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization. Working at Azurity offers a unique opportunity that combines the fast pace and growth opportunities of a startup with intellectual rigor and creativity.

As part of the Medical Affairs team, The Medical Science Liaison (MSL) serves as a scientific expert and strategic partner within the Medical Affairs team, engaging with healthcare professionals (HCPs), academic institutions, and other stakeholders to advance scientific exchange and support the medical strategy. The MSL will play a key role in identifying insights, supporting evidence generation, and facilitating access to innovative therapies across Europe.

Principle Responsibilities

• Be a strategic partner - gather and leverage insights for an impactful contribution to launch excellence, integrated evidence generation plans, integrated product strategy and subsequently the medical strategy.
• Utilize knowledge of assigned therapeutic area and Azurity products to serve as the Medical, Clinical and Scientific expert to field matrix colleagues. Identify data gaps, data generation opportunities (including RWE and implementation science, precision medicine), and key unmet needs and opportunities to help improve patient access and outcomes.
• Ensure appropriate identification and mapping of external stakeholders, aligned to the medical strategy. Able to create personalized, flexible engagement strategies and plans, leveraging multiple channels and tailored content to meet the changing needs of external stakeholders.
• Personalize and expand external stakeholder engagement beyond Healthcare Professionals. Support and contribute to innovative partnership models for shared ownership in transforming clinical practice. Apply foundational impactful Scientific Engagement principles in stakeholder interactions in alignment with medical strategy and portfolio/pipeline prioritization.
• Respond to unsolicited requests for information from stakeholders by sharing appropriate data regarding marketed and pipeline compounds in a timely, compliant, and stakeholder-focused manner.
• Manage administrative responsibilities in a timely manner (customer relationship management tool, compliance training and other modules, expense reporting, etc.).
• Promote and adhere to Ethics and Compliance Professional Practices Policy (P3).
• Provide internal training to commercial and medical colleagues on disease areas and product science.
  
  

Qualifications And Education Requirements

• Doctoral-level qualification (PharmD, PhD, MD) required.
• Minimum 1–3 years of experience in a Medical Affairs or clinical/scientific role, preferably within the pharmaceutical or biotech industry.
• Strong knowledge of the European healthcare environment (medical practice, clinical decision making and healthcare systems)
• Deep understanding and knowledge of local regulations and codes of practice for pharmaceutical industry, in particular as they apply to the non-promotional activities of this role.
• Proven ability to interpret and communicate complex scientific data.
• Excellent organizational, interpersonal, and communication (verbal, written, presentation) skills with flawless attention to detail
• Possess collaborative teamwork and leadership skills; capable of building successful relationships
• Ability to thrive in a fast-paced, dynamic environment
• Fluent in English; additional European languages (French, Spanish, German, Italian, etc) are a plus.
• Willingness to travel extensively (up to 60%) across Europe.
  
  

Preferred Experience

Experience in one or more of the following therapeutic areas: oncology, immunology, endocrinology, cardiometabolic diseases, or rare diseases.

Familiarity with digital engagement tools and omnichannel medical communication strategies.

Prior involvement in clinical trial support or RWE initiatives.