The Medical Science Liaison (MSL) is a field-based scientific and clinical expert required to reside within the assigned geographic territory (Northeast, Southeast, Midwest, South Central, Mountain/Southwest or West Coast) and serves as the primary communicator of our science for that region. The MSL will establish and maintain relationships with healthcare professionals, key opinion leaders, academic institutions, and professional societies, providing fair, balanced, and compliant scientific exchange on topics including disease state, current therapeutic landscape, as well as AiCuris clinical stage antiviral agents and products in development. As we prepare for our 2026 launch of pritelivir, the MSL will play a vital role in understanding the treatment landscape, building relationships with key external experts, supporting clinical development activities, and gathering insights that will inform our medical and commercial strategies.
Identify, gain access to, and develop professional customer-centric relationships with key opinion leaders (KOLs), external experts, and healthcare providers within assigned geography.
Develop, execute, and maintain comprehensive territory plans that align with medical and scientific objectives, with emphasis on quality and strategic impact.
Responding to unsolicited medical and scientific inquiries from external stakeholders in a timely and compliant manner.
Support clinical research initiatives, including site identification and evaluation, investigator recruitment and relationships, investigator meetings, and external collaboration management
Support both company-sponsored and investigator-initiated studies aligned with medical strategy.
Identify educational gaps and data needs to inform research and development strategy.
Collaborate compliantly with internal stakeholders, including Medical Affairs teams, R&D, Global Medical Affairs, Clinical Operations, and commercial partners.
Work in a compliant manner with field commercial teams, including market access, to develop and execute account plans that support shared business objectives.
Ensure compliance with corporate policies, regulatory guidelines, healthcare compliance requirements, and Medical Affairs SOPs.
Maintain accurate and timely documentation of healthcare provider interactions and field activities in the company support CRM.
Doctorate degree in health science or clinical discipline (PharmD, MD, DO, PhD, DNP, or equivalent advanced degree)
Clinical, scientific research, pharmaceutical industry, or equivalent therapeutic area experience
Strong understanding of clinical study design, research methodology, statistics, and regulatory environment
Proficiency in leveraging data, insights, and digital tools to optimize territory strategy
Valid US driver's license required
Ability to travel extensively (up to 70-75% of the time) by car, train, and plane domestically
Scientific excellence, a collaborative working environment and the passion to improve the lives of patients defines our work. With us, you can work together with innovation awarded experts with the proven ability to translate science into commercial success. We encourage people to grow and strongly support individual development and learning opportunities.
Embracing flexible working accommodations, we enable our people to integrate business into their personal life.
Benefits: Competitive comprehensive benefit plan
Our pivotal phase 3 candidate Pritelivir aims to address recurrent and resistant HSV infections in a broad population of patients with weakened immune systems. We believe in a culture of trust and transparency, where feedback is considered an opportunity to contribute to each other's personal and professional growth.