Identify unmet medical needs for respective therapeutic areas based on scientific data, clinical evidence, KME insights, and evolving standards of care
Develop and implement local medical plans for pipeline assets, aligned with Global and BIR priorities
Lead cross-functional medical planning, ensuring integration with Clinical Development, Regulatory, Market Access, and Commercial teams
Lead local medical input into evidence generation strategy, such as real-world evidence, registries, and investigator-initiated research
Collaborate with Global/BIR/Development teams to shape Phase IV and post-approval evidence plans
Create scientific quality of study concepts, protocols, and key medical documents. Responsible for the study execution
Disseminate clinical study data at relevant medical congress to facilitate understanding of pipeline assets
Manage strategic relationships with Key Medical Experts (KMEs) to drive medical strategy and evidence generation
Provide scientific expertise and educational support to internal stakeholders
Requirements
PhD in scientific discipline or equivalent scientific expertise