• 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.

• Establish and maintain strategic relationships with Key Opinion Leaders (KOLs), academic institutions, community oncology practices, and health and hospital systems to enhance awareness of the company’s diagnostic solutions. • Develop, update, and deliver scientific and medical education (e.g., slide decks, abstracts, manuscripts, and clinical data presentations) to healthcare professionals and stakeholders, ensuring accurate and effective communication of emerging scientific evidence and clinical utility. • Lead and coordinate scientific engagement at academic and professional forums, including national and regional congresses, symposia, grand rounds, and continuing medical education (CME) programs, aligning content with unmet clinical needs and organizational priorities. • Serve as a subject matter expert for internal cross-functional partners (e.g., commercial, market access, clinical development, and marketing teams) by providing insights on clinical utility, biomarker strategies, competitive landscape, and evolving standards of care. • Provide regular scientific updates and educational briefings to internal stakeholders through internal presentations and cross-functional meetings to ensure alignment on emerging evidence and medical strategy. • Collaborate with cross-functional partners to identify opportunities for strategic KOL engagement, including educational initiatives, clinical research collaborations, and outreach to healthcare systems, academic institutions, health and hospital systems, and payer stakeholders to support appropriate product adoption. • Serve as Medical Affairs lead for Clinical Advisory Boards, including strategic planning, scientific agenda development, and facilitation of expert discussions. • Ensure that insights generated from advisory boards are captured and translated into actionable medical and business strategies. • Identify opportunities to generate meaningful scientific insights through engagements with KOLs, focus groups, and advisory interactions, helping inform medical strategy, clinical development priorities, and product innovation. • Maintain deep scientific expertise in oncology care pathways, including cancer patient-management algorithms, molecular testing strategies, and the clinical utility of laboratory-developed tests (LDTs) and biomarker-driven diagnostics. • Respond to complex medical and scientific inquiries from healthcare providers and internal stakeholders in a timely, accurate, and compliant manner, ensuring appropriate documentation in customer relationship management (CRM) systems. • Support generation and dissemination of scientific evidence, including collaboration on research initiatives, abstract development, and manuscript preparation for peer-reviewed journals and scientific conferences. • Capture and communicate voice-of-customer (VOC) insights from the field to inform medical strategy, product development, and cross-functional decision-making. • Travel extensively within the assigned territory, with additional travel to national meetings and meetings as required (75%). • Perform other duties as assigned to support Medical Affairs objectives and organizational priorities.

• Proactively identify key regional healthcare decision makers (HCDMs) • Serve as the primary medical liaison between AbbVie and the HCDM • Build strong relationships to understand customer needs • Facilitate generation of real-world evidence (RWE) consistent with approved therapeutic area medical planning • Participate across assigned therapeutic area and healthcare landscape strategic committees • Customize communication of scientific, health outcomes, and health policy information to HCDMs and influencers • Document and communicate meaningful observations which lead to insights on a regular basis • Identify relevant emerging scientific, health economic, and health policy trends • Primary interface and initial point of contact for small-scale, RWE opportunities with regional level HCDMs • Anticipate, identify and address population-level scientific, outcomes research, and health policy needs of customers • Facilitate scientific exchange between AbbVie Medical Leadership and accounts • Maintain and enhance clinical, scientific, and healthcare landscape expertise • Participate in various therapeutic advisory activities involving marketed and investigational products

• Serve as the primary interface with clinical trial sites, collaborating with Clinical Development and Operations to ensure high-quality study execution, specifically clinical trial enrollment. • Participate in planning and setup for your region, aligning with local colleagues and CROs. • Develop deep expertise in multiple therapeutic areas, including inflammatory bowel disease. • Act as the regional subject matter expert and credible scientific leader. • Build and maintain relationships with opinion leaders, clinical investigators, and study staff within your region. • Provide scientific support to Clinical Development, Medical Affairs, Commercial, and other teams. • Support activities such as local, regional, national, and as needed, international, congresses, share clinical and scientific insights with cross-functional teams. • Operate ethically and comply with all laws, regulations, and policies.