Principal Medical Science Liaison - Rare Disease - West

Role Overview This position is ideally based remotely in the United States, with a preference for candidates located on the West Coast (e.g., CA, CO, UT, AZ, and neighboring states). Proximity to a major travel hub is advantageous to support frequent regional travel. The role involves covering approximately one-third of the continental United States and engaging with healthcare professionals (HCPs) and key opinion leaders (KOLs) at leading hospitals and specialized centers. The position offers flexibility with a hybrid or fully remote work environment. Key Responsibilities Act as a field-based representative of the Medical Affairs team, fostering scientific exchange with KOLs, investigators, and other stakeholders in the medical community. Identify and address the educational and professional needs of KOLs, healthcare providers, academic thought leaders, payers, and relevant government organizations in alignment with strategic plans. Communicate the organization's product portfolio compliantly and effectively, collaborating with Medical Communications to develop and deliver standard responses. Collaborate with Medical, Clinical Development, and Clinical Operations teams to design and execute scientific programs, advisory boards, and related initiatives. Partner with Medical and Commercial colleagues to provide scientific support for payer organizations. Offer support to investigators involved in clinical and observational studies, including investigator-sponsored research. Stay updated on relevant disease areas, indications, and best practices for Medical Science Liaisons (MSLs). Maintain detailed and compliant records of KOL/HCP interactions, insights, and feedback within the customer relationship management system (e.g., Veeva). Deliver training sessions for internal teams, including Medical and Commercial personnel, as needed. Participate in cross-functional projects, such as the development and implementation of standard operating procedures (SOPs). Identify and implement process improvements to align with evolving business needs. Qualifications Advanced degree (e.g., MD, PharmD, or PhD) required Minimum of 5-8 years of MSL experience, with a focus on rare diseases and field-based scientific exchange. Background in clinical trial support is a plus. Launch Experience Previous Experience supporting a Rare Disease Product Preference for candidates with experience in early-stage biopharmaceutical companies. Strong communication skills, with a proven ability to engage and educate stakeholders in both virtual and in-person settings. Demonstrated ability to manage priorities and resources effectively, with a proactive problem-solving mindset. Familiarity with medical guidelines, regulatory frameworks, and compliance standards. Willingness to travel extensively (up to 80% of working time) and attend occasional weekend meetings. Valid driver's license in good standing.

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