About this role
Join Grifols, a global healthcare company since 1909 working to improve health worldwide. Leaders in plasma-derived medicines and transfusion medicine, operating in over 110 countries. The role supports scientifically-sound medical plans in Pulmonology and Critical Care therapeutic areas.
Develop and lead Medical Affairs initiatives aligned with global and US medical plans to drive innovation and company goals. Provide medical guidance to internal stakeholders and educate external customers on therapeutic areas and Grifols products. Build relationships with key opinion leaders to gather insights for strategy and portfolio.
Serve as therapy area expert for Scientific Innovation Office and commercial functions. Participate in advisory boards, speaker trainings, symposia, and conferences. Review promotional materials, publication plans, and investigator research proposals.
Opportunity is US-based with 20% national/international travel. Can be based in RTP, North Carolina or remote home office. Partner across patient advocacy, regulatory, HEOR, and market access to support US and global needs.
Requirements
- MD with at least 8 years experience in Pulmonology and Critical Care, Board Certification preferred
- Prior academic position preferred
- Knowledge of medical affairs within plasma/pharmaceutical industry experience preferred
- Advanced analytical and strategic thinking skills
- Demonstrated exceptional interpersonal and communication (oral and written) skills
- Excellent relationship building skills and ability to collaborate with internal and external stakeholders
- Results-driven and committed to excellence in the achievement of objectives
- Willingness to travel within the US and globally (15-20%)
Responsibilities
- Serve as the therapy area expert for internal and external stakeholders
- Support development of global and US medical affairs plans in alignment with business objectives
- Build and maintain relationships with scientific thought leaders in Pulmonology and Critical Care
- Provide product and disease-specific education and training to internal stakeholders and external customers
- Participate in and/or facilitate advisory boards, speaker training meetings, symposia, and webinars
- Review promotional materials and medical information letters to ensure medical accuracy
- Contribute to the development and execution of publication plans and strategies
- Review investigator initiated research concepts and proposals and make funding recommendations
Benefits
- US-based role with option for RTP, North Carolina or remote home office
- 20% national/international travel to conferences and events
- Work with global leader in plasma-derived medicines and innovative healthcare solutions
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