Medical Affairs Medical Director- Pain

Role Summary

The Medical Director, Medical Affairs Strategy will provide medical leadership for the US Pain team and will be responsible for developing the medical strategy and medical plan as well as executing against the medical plan for US Pain. This role will lead a team that will collaborate closely with cross-functional groups to ensure that scientific and medical strategies are aligned with broader corporate and key stakeholder needs as well as ensuring the voice of the patient and medical community is integrated into product strategies.

Responsibilities

• Develops medical affairs plans, including Launch and Life Cycle Management study plans
• Critically interprets scientific data, determines the potential impact of new research on clinical practice, and uses scientific and clinical data to formulate frameworks and disease management approaches
• Provides input from medical community into clinical development and commercial strategies
• Effectively communicates scientific data through presentations and publications
• Ensures country/regional insights and needs are considered in global medical strategies and activities
• Provides scientific input and expertise as a medical reviewer and supports the development of global medical, commercial, regulatory, and reimbursement documents
• Performs/oversees medical/scientific training for Medical, Commercial, and other internal stakeholders
• Reviews investigator-sponsored study (ISS) proposals and other research grants
• Supports projects as assigned by the Sr Med Dir including supporting Medical Symposiums, Webinars, Videos, Medical Education Content development and Training, and Medical Society relationships
• Leads Medical Advisory Boards
• Supports Commercial Speaker Training
• Supports the development of the Integrated Evidence Generation Plan
• As a people manager within the organization, may have financial accountabilities and human resource responsibilities for assigned staff

Qualifications

• M.D. degree or equivalent (e.g., D.O.)
• Typically requires a minimum of 5 years post US/UK/Canada residency/fellowship academic clinical experience
• Typically requires at least 3-5 years of industry experience working in the biotech/pharma/implantable medical device industry or the equivalent combination of education and experience
• Typically requires experience in a Medical Affairs function and in the analysis of research (clinical) data and publications; working knowledge of biostatistics as well as scientific and clinical research methods, and clinical study design
• Orthopedic or Surgical sub-specialty highly desirable

Knowledge And Skills

• Deep understanding of US medical, regulatory and commercial (including payer) environments
• Excellent understanding of government and industry guidelines, regulations, laws, etc., for appropriate scientific/medical exchange and communication with key external stakeholders (e.g., healthcare providers, payers, advocacy bodies)
• Deep understanding of market access in the US
• Excellent written and oral communication skills to influence others internally/externally
• Critical ability to develop relationships in a highly matrixed environment, as well as external relationships with global, regional and local thought leaders and industry experts
• Ability to engage in positive dialogue and resolve conflicts in a constructive manner
• High fluency/digital literacy in use of PowerPoint