· Develop and execute a territory scientific engagement plan aligned with country and regional medical priorities, stakeholder needs and agreed outcomes.
· Build and sustain trusted, peer-to-peer scientific relationships with leading specialists, investigators, healthcare professionals, scientific societies and relevant healthcare decision-makers.
· Conduct high-quality, balanced and non-promotional scientific exchange, responding accurately to unsolicited medical questions and adapting communication to the needs of expert audiences.
· Maintain deep and current scientific knowledge; critically appraise clinical evidence, treatment pathways, emerging data and changes in the healthcare environment.
· Gather, document, synthesize and communicate actionable field insights, unmet needs, evidence gaps and barriers to care that can inform medical strategy and execution.
· Contribute to prelaunch and launch readiness by mapping priority stakeholders and institutions, identifying scientific knowledge gaps, supporting educational initiatives and monitoring healthcare-environment readiness.
· Develop strong engagement with hospital-based specialists, multidisciplinary teams, institutional pharmacists, diagnostic stakeholders and decision-makers involved in complex patient-care pathways.
· Identify barriers to evidence adoption and appropriate patient management, and propose compliant medical actions that address genuine stakeholder needs.
· Support medical education, advisory boards, congress activities and scientific meetings, ensuring scientific rigor, appropriate governance and compliant execution.
· Support evidence-generation activities, investigator-initiated research, site identification and feasibility discussions, as applicable and within role-defined responsibilities.
· Collaborate with Medical, Clinical Development, Regulatory, Market Access and Commercial colleagues in a matrix environment while protecting the independence and non-promotional mandate of Medical Affairs.
· Maintain accurate stakeholder and activity records in approved systems and fulfill all pharmacovigilance, product quality and compliance reporting obligations within required timelines.