Medical Science Liaison

Medical Affairs LOCATION: Fully Remote – frequent travel to the Midwest (Chicago, MN, Michigan, Milwaukee, etc…) Humacyte Inc (Nasdaq: HUMA) is developing a disruptive biotechnology platform to deliver universally implantable bioengineered human tissues, advanced tissue constructs, and organ systems designed to improve the lives of patients and transform the practice of medicine. The Company develops and manufactures acellular tissues to treat a wide range of diseases, injuries, and chronic conditions. Humacyte’s initial opportunity, a portfolio of Acellular Tissue Engineered Vessel (ATEVs), is currently approved for use in vascular trauma repair and is in late-stage clinical trials targeting multiple other applications including AV access for hemodialysis and peripheral arterial disease. Preclinical development is also underway in coronary artery bypass grafts, pediatric heart surgery, treatment of type 1 diabetes, and multiple novel cell and tissue applications. Humacyte’s 6mm ATEV for urgent arterial repair following extremity vascular trauma also received the RMAT designation. Humacyte, Inc. is bringing to market a once in a generation scientific technology platform, bioengineering readily available and universally implantable product opportunities focused on improving lives of patients and transforming the practice of medicine. Initially developing a portfolio of human acellular vessels (HAVs), to target multiple vascular markets including trauma, arteriovenous access for hemodialysis, peripheral arterial disease, and coronary artery bypass grafting. This position acts as a bridge between Humacyte, KOLs, physicians, scientists, patient societies, CROs and other groups and provides scientific and clinically sound information about Humacyte products. This is an external facing position that interfaces with the medical community, key opinion leaders and regulatory agencies as applicable. Responsibilities Execute territory plans in alignment with Medical Affairs plans. Identify and communicate key clinical and research issues and insights from KOLs to appropriate departments. Collaborate with clinical team in identifying clinical investigators and partner with Clinical team to educate investigators and sites through communication of relevant medical/scientific data. Serve as a subject matter expert for internal cross-functional teams, as it relates to the medical/scientific data for our products. Serve as a subject matter expert for regional external meetings, as it relates to the medical/scientific data for Humacyte products, in a fair and balanced manner. Provide scientific support and participate in medical education for healthcare professionals (HCPs) through on-site presentations at healthcare institutions, investigator meetings, national conferences, advisory boards, or regional meetings. Collaborate in the development of educational materials for delivery at conferences, KOL engagement activities, and other speaking engagements. Partner with the internal stakeholder teams to develop medical/scientific materials that meet regulatory guidelines and provide key medical/scientific data to desired audience. Review for technical/medical/scientific accuracy written or electronic materials related to Humacyte products to ensure accuracy and compliance to regulatory requirements including, but not limited to, clinical trial protocols, study tools and clinical study reports (CSR) assist with Safety operations, reporting and exposure tracking. collaborate with personnel on Health Economics projects. assist with Regulatory Affairs operations and discussions. Qualifications Work with CRO clinical research associates (CRAs) to ensure that investigators and site staff have a thorough understanding of the investigational product, protocol eligibility criteria, and all study procedures. Keep abreast of the latest research and developments in the medical/scientific fields related to our product and indications. Outstanding presentation and training skills Demonstrated expertise in developing training tools appropriate for high level stakeholders in the scientific and/or medical communities Able to communicate effectively in English, both verbally and in writing Basic computer skills required, such as knowledge of MS Word, Excel, PowerPoint, and Outlook Self-motivated and organized critical thinker with solid interpersonal and business communication skills Adheres to company and facility specific policies and procedures, including SOP, training and meeting requirements Willingness to travel within assigned region, this may include frequent air travel MD/DO, PhD, DMSc, or NP/PA degree required. Preferably Midwest-based, as the territory covered will include frequent travel to Chicago, MN, Milwaukee, Michigan and other nearby states. Willingness to travel – 50%+ A minimum of 2 years of experience in a Medical Science Liaison or equivalent position required. Benefits Stock Options Medical, Vision and Dental Plans Company Paid Long Term/Short Term Disability Company Paid Life Insurance 10 Company Designated Holidays + 2 Floating Holidays Paid Parental Leave Policies S. employment sponsorship and does not accept unsolicited resumes from 3rd party firms and/or agency recruiters. Humacyte is an equal opportunity employer and is committed to providing equal employment opportunities without regard to age, race, religion, sex, sexual orientation, gender identity, national origin, Veterans status, disability and/or other protected class characteristics. Additionally, Humacyte is committed to achieving its business objectives in compliance with all federal, state and local law. #J-18808-Ljbffr HUMACYTE GLOBAL INC