Medical Science Liaison

1 week ago


Plymouth Meeting, Pennsylvania, United States Inovio Pharmaceuticals Inc Full time
About Inovio Pharmaceuticals Inc

Inovio Pharmaceuticals Inc is a biotechnology company dedicated to developing and commercializing DNA medicines to address infectious diseases, cancer, and diseases associated with HPV. Our DNA medicines in development utilize our proprietary smart device to produce immune responses against targeted pathogens and cancers. For more information, visit our website.

Job Summary

We are seeking a highly skilled Medical Science Liaison to support our US Medical Affairs team in executing our Medical Affairs strategy. The successful candidate will ensure accurate, robust, and appropriate medical/scientific exchange of knowledge and clinical expertise with US stakeholders, primarily focused on our Recurrent Respiratory Papillomatosis program and DNA Medicine Platform.

Key Responsibilities
  • Execute the company's Field Medical Affairs' strategies/tactics for Inovio's Recurrent Respiratory Papillomatosis program and DNA Medicine Platform.
  • Maintain in-depth understanding of the disease state, product, competitors, marketplace, related medical areas, and regulatory guidelines.
  • Identify and foster scientific relationships with key opinion leaders (KOLs) and other healthcare professionals (HCPs) within assigned territory.
  • Act as the primary scientific resource for HCPs and conduct scientific exchange in a compliant manner.
  • Work closely with the Account Directors to identify and appropriately engage with medical influencers/decision makers to help educate the payer and market access community on Inovio and related disease states.
  • Provide timely intelligence and insights on emerging clinical/scientific trends back to the organization, along with opportunities aimed at better meeting the needs of the external healthcare community.
  • Communicate relevant information to internal stakeholders in order to define, update, and support medical strategies.
  • Act as a contributing partner in developing USMA strategy and cross-functional plans tactics.
Requirements
  • Advanced scientific degree (PhD, PharmD, or MD) required.
  • Minimum of 5 years of Medical Affairs experience (ideally as an MSL and preferably in the biotech industry) required.
  • Experience working in rare or orphan disease space.
  • Payer and HEOR experience required.
  • Excellent written and oral communication skills, including strong formal presentation skills.
  • Excellent planning and organization skills, especially in territory management and KOL development.
  • Strong interpersonal skills commensurate with the need to work closely with both external physicians/scientists and numerous internal business partners.
  • Ability to integrate scientific data into real-life practice to meet customer/audience needs, adapting interpersonal style to particular situations and people.
  • Ability to maintain the highest degree of integrity, represent the company's high ethics, moral behavior, and professionalism.
  • High proficiency in problem-solving and strong scientific analytical skills.
  • Willingness/ability to travel up to 60-80%.
  • Knowledge of pharmaceutical/healthcare market, acceptable practices, and related regulations is required.
  • Advanced understanding of clinical/medical science is required.
  • Strong understanding of regulatory and professional guidelines associated with the compliant dissemination of medical information and HCP engagement (OIG, FDA, AMA, ACCME, and PhRMA guidelines).
  • Ability to think strategically about communicating to different stakeholders through all scientific engagement channels.
  • Strong, consistent record of executing strategically and tactically in a highly matrixed environment composed of cross-functional, dynamic teams.
  • Ability to critically evaluate scientific literature and evolving competitive landscape.
  • Ability to operate independently with minimal supervision.


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