Medical Director, Scientific Affairs – Milvexian

Johnson & Johnson Johnson & Johnson · Pharma · Titusville, NJ +1

Medical Director, Scientific Affairs for milvexian, responsible for designing and executing US Scientific Affairs initiatives including medical education, advocacy, evidence dissemination, and generation. Collaborates with internal and external partners, manages pharmacovigilance, promotional review, and regulatory documents. Serves as a disease area expert, engages with thought leaders and patient advocacy groups, and oversees medical education and training activities.

What you'd actually do

  1. design and execution of U.S. Scientific Affairs initiatives supporting milvexian (i.e., medical education programs, advocacy initiatives, evidence dissemination, and evidence generation)
  2. Strong collaboration with internal and external business partners including regulatory, brand marketing, Real World Value & Evidence (RW V&E), Research & Development, Global Medical Affairs, epidemiology, clinical investigators, advocacy organizations, and key external experts.
  3. Responsibility for pharmacovigilance, medically important results assessments (MIRA) evaluations, promotional review committee assignment, label revisions, speaker and sales representative training, and other similar activities.
  4. Serve as a disease area scientific and medical expert and resource for internal audiences
  5. Provides clinical and scientific leadership through interaction with internal and external experts, including:

Skills

Required

  • Master’s degree
  • 8 years experience in clinical practice, industry, academia and/or related area
  • Pharmaceutical industry experience

Nice to have

  • advanced degree
  • Experience and knowledge of cardiovascular disease or anticoagulation, drug development, and Medical Affairs
  • Indirect team leadership
  • Demonstrated success leading a clinical/scientific cross functional team
  • Understanding of US healthcare dynamics
  • Analytical Reasoning
  • Business Requirements Analysis
  • Clinical Research and Regulations
  • Clinical Trials Operations
  • Communication
  • Developing Others
  • Digital Culture
  • Digital Literacy
  • Healthcare Trends
  • Inclusive Leadership
  • Leadership
  • Medical Affairs
  • Medical Communications
  • Medical Compliance
  • Product Strategies
  • Stakeholder Analysis
  • Strategic Thinking
  • Workflow Analysis

What the JD emphasized

  • Master’s degree required
  • A minimum of 8 years experience obtained in clinical practice, industry, academia and/or related area is required
  • Pharmaceutical industry experience is required