The Vice President of Medical Affairs Therapeutic will provide strategic medical leadership across all CSL products, pipeline and inline.
This is a critical role to drive medical strategy and execution excellence, enabling R&D strategy and enabling commercial growth objectives through evidence generation, thought leadership, scientific engagement and product expertise.
Main Responsibilities & Accountabilities Oversees and directs pipeline TA Medical Directors' activities in developing and executing comprehensive medical plans to product development and Go-to-Market Strategies for all CSL Behring pipeline products.
Oversees and directs inline Medical Directors' activities providing subject matter expertise to all countries for all CSL Behring inline products.
Oversees development and execution of comprehensive IEGPs, coordination of all evidence generation activities, and development of ISS scope documents across Tas to ensure strategic, and high quality data generation and publications from all types of evidence throughout lifecycle for all CSL Behring pipeline and inline products.
Provides subject matter and medical expertise input into TA strategies ensuring close collaboration with R&D to deliver data and a label to support TPPs and reflect the value required to enable speedy access to patients.
Functions as the scientific medical expert internally and externally with national and international stakeholders.
Serves as a collaborator and key stakeholder to the Heads of Medical Affairs in the US and International, Global Commercial Development, Global Market Access, Global Clinical R&D, Global Pharmacovigilance and Promotion Review Committee (PRC) on medical aspects of the company's products.
Ensures strong, efficient and effective Medical Affairs operations and directs the activities of the TAs supporting all CSL products, pipeline and inline, to assure established performance objectives are met.
Ensures both pipeline TA Medical Affairs and Inline Medical expert teams are properly staffed to appropriately serve as an internal scientific expert for all disease states and products.
Ensures all personnel are trained and strong in medical, scientific, and regulatory knowledge as well as industry research and trends.
Drives development plan for direct reports and guides development of their teams.
Provides final review and approval of scientific communications on company products and therapeutic areas.
Qualifications & Experience Requirements MD with 15+ years of pharmaceutical/biotherapeutics industry experience.
Clinical experience, preferably in a specialty relevant to CSL's therapeutic areas/products.
8+ years of Executive Medical Affairs Leadership experience.
Experience building and leading and managing teams in a global organization.
Strong capabilities in medical strategy, evidence generation and scientific engagement.
Influential leader who builds relationships across stakeholder types.
Executive presence with ability to communicate complex data persuasively and relate study results and knowledge of therapeutic area to industry-specific applications.
Strong working knowledge across multiple therapeutic areas and products.
About CSL Behring CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases.
Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas.
We want CSL to reflect the world around us As a global organization with employees in 35+ countries, CSL embraces diversity and inclusion.
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