Senior Director, Medical Affairs, Pipeline Hematology

4 weeks ago


King of Prussia, Pennsylvania, United States CSL Behring Full time

The Senior Director, Global Medical Affairs Pipeline Hematology is a key member of the Therapeutic Area Leadership Team (TALT), contributing to the cross-functional development of TA strategies and individual global product strategies.

Main Responsibilities & Accountabilities

  • Oversees and directs pipeline TA Medical Directors' activities in developing and executing comprehensive medical plans to support product development and Go-to-Market Strategies for TA pipeline products ensuring full integration with marketing and market access and alignment with regions and countries (as needed).
  • Oversees development and execution of comprehensive disease awareness programs and Integrated Evidence Generation Plans (IEGPs) ensuring high-quality publications from all types of evidence throughout development up to launch.
  • Provides global strategic medical affairs expertise to the TA and participates in the cross-functional development of TA strategy and individual product plans as a TALT member ensuring a deep understanding of the diseases the TAs are currently or planning to participate in.
  • Functions as the TA scientific medical expert internally and externally with national and international stakeholders.
  • Serves as a collaborator and key stakeholder to the relevant senior leaders in Medical Affairs in the US and International, Global Market Access, Global Clinical, Global Regulatory, Global Research, and Global Pharmacovigilance.
  • Ensures strong, efficient, and effective Medical Affairs operations and directs the activities of the TA to assure established performance objectives are met in a fully compliant manner.
  • Ensures TA Medical Affairs is properly staffed to appropriately serve as an internal scientific expert for relevant disease states and pipeline products and that all personnel are trained and strong in medical, scientific, and regulatory knowledge as well as industry research and trends.
  • Ensures the support of the internal TA training of medical affairs colleagues in the regions and countries.

Qualifications & Experience Requirements

  • MD with 12+ 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 matrixed teams in a global organization.
  • Strong capabilities in clinical research, evidence generation, scientific engagement, and a demonstrated record of influential leadership.
  • Executive presence with the 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.


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