Medical Device Science Liaison - US Remote

Responsibilities

• Leverage scientific expertise and market knowledge to establish and build professional relationships and engage with HCPs (including academic physicians, community physicians, medical experts, nurses, and other healthcare professionals) and other thought leaders as aligned with medical strategy.
• Engage with customers in the field - customer engagements may include but are not limited to emerging data discussions, clinical trial activities, exploration of areas of unmet medical need, pipeline discussions, educating on disease state and product, and capturing medical insights through all stages of the product lifecycle.
• Responds in a timely manner to unsolicited scientific inquiries, delivering balanced, accurate information in accordance with available scientific evidence and company standards.
• Identify opportunities for partnership with academic centers, centers of excellence, and/or systems of care to drive impact.
• Support scientific engagements, attend congresses, run advisory boards, and other Medical Affairs initiatives.
• Identify opportunities to involve HCPs or MEs when a specific medical need is identified (e.g., publications, clinical trial participation, etc.).
• Engage with external investigators.
• Manage unsolicited research inquiries.
• Works cross-functionally with Clinical Research, R&D, and other operations teams.
• Supports company-sponsored trials.
• Represents Rout 92 Medical and provides leadership at scientific conferences to gather and understand new scientific information relevant to the company and scientific community.
• Organizes and leads stakeholder meetings, including symposia, advisory boards, and investigator meetings.
• Maintains an in-depth knowledge of internal policies and external regulations (e.g., travel policy, expense policy, state and local laws, institutional policies) and how they affect day-to-day responsibilities.
• Executes all administrative responsibilities and training (e.g., e-mail, expense reports, compliance modules, etc.) in a timely manner.

Qualifications

• Strong relevant clinical experience (e.g., PA-C) in the neuro-interventional space.
• Experience with Microsoft Word, Excel, PowerPoint, and the utilization of computers and remote technologies.
• Current working knowledge of FDA, OIG, HIPAA, and other compliance regulations and guidelines relevant to industry interactions with healthcare professionals.
• Ability to travel up to 70% with some international travel requiring a valid passport.
• Significant experience giving presentations is highly preferred.
• Demonstrated understanding of clinical trial management.