Key skills
Collaboration
About this role
Role Overview
- 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
- Advanced scientific degree (MD, PhD, PharmD) preferred
- 3 years of working experience in Medical Affairs, Clinical Development, or related pharmaceutical roles
- Proven experience in medical strategy development, evidence generation, and cross-functional collaboration
- Fluent in English; local language proficiency required as applicable
- Strong scientific expertise in immunology, or relevant therapeutic areas
- Strategic thinking and decision-making capability
- Ability to synthesize complex scientific data into clear strategic direction
Benefits
- Professional development opportunities
- Flexible work environment
- Commitment to diversity, equity, and inclusion