Nobelpharma America, LLC

• Build and maintain strong, credible, long-term relationships with key opinion leaders (KOLs), specialists, investigators, patient advocacy organizations, and centers of excellence across assigned territories. • Conduct high-quality scientific exchange with external stakeholders to communicate clinical data, disease-state information, treatment insights, and emerging research in a fair and balanced manner. • Identify, map, and prioritize key stakeholders in alignment with medical strategy and organizational objectives. • Represent Nobelpharma America, LLC at scientific congresses, educational programs, advisory activities, and medical meetings. • Maintain a high level of clinical, scientific, and technical expertise in relevant therapeutic areas and company-supported products. • Deliver compliant, non-promotional scientific presentations and educational support to external experts and internal stakeholders. • Respond to unsolicited medical inquiries with timely, accurate, and evidence-based information in accordance with company policy and compliance standards. • Support medical and clinical initiatives, including clinical trial awareness, site identification, and investigator-initiated study activities, as appropriate. • Gather, synthesize, and communicate field insights related to treatment patterns, unmet medical needs, scientific trends, and the competitive landscape. • Share actionable insights with internal stakeholders to inform medical strategy, evidence generation, and broader business planning. • Collaborate effectively with cross-functional teams including Medical Affairs, Medical Information, Pharmacovigilance, Market Access, and Commercial Operations. • Support internal initiatives such as speaker training and sales training by ensuring scientific accuracy and appropriate clinical context. • Partner with field leadership and other customer-facing roles while maintaining clear boundaries and full compliance with all applicable regulations and company policies. • Conduct all activities in accordance with legal, regulatory, ethical, and company compliance requirements. • Maintain current knowledge of scientific literature, treatment guidelines, healthcare trends, and developments within relevant therapeutic areas. • Perform additional duties and special projects as needed to support Medical Affairs and company priorities.