HUMACYTE GLOBAL INC logo

Medical Science Liaison

HUMACYTE GLOBAL INC

Chicago, IL; Detroit, MI; Minneapolis, MN; Milwaukee, WIRemotePosted 24 days ago
Full TimeEntry LevelMedical AffairsBiotechnology
Original posting ↗

Summary

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.

Job description

Major Accountabilities

  • Utilizing a strong understanding of Humacyte products and our core therapeutic areas, engage external stakeholders and communicate the benefits of our products to their applicable patients.
  • Develop a network of Key Opinion Leaders (KOL) and KOL engagement strategies by collecting insights and medical/scientific data.
  • 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).
  • Utilize clinical expertise to assist with Safety operations, reporting and exposure tracking; collaborate with personnel on Health Economics projects; assist with Regulatory Affairs operations and discussions.
  • 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.
  • Provide detailed reports of interactions with external stakeholders.
  • Keep abreast of the latest research and developments in the medical/scientific fields related to our product and indications.

Special Competencies

  • Outstanding and demonstrated communication and influencing skills
  • Demonstrated ability to develop strong relationships with individuals at all levels
  • Outstanding presentation and training skills
  • Demonstrated expertise in developing training tools appropriate for high level stakeholders in the scientific and/or medical communities

General Competencies

  • Able to communicate effectively in English, both verbally and in writing
  • Excellent communication and interpersonal skills
  • Possess a positive roll-up-the-sleeves attitude and optimistic outlook
  • Strong ability to work in a fast-paced team environment with fluctuating priorities, and collaborate effectively with others
  • Excellent organizational and time management skills with ability to set own priorities in a timely manner
  • High degree of flexibility and adaptability
  • Basic computer skills required, such as knowledge of MS Word, Excel, PowerPoint, and Outlook
  • Must be able to work as needed to meet tight deadlines and at peak periods
  • Self-motivated and organized critical thinker with solid interpersonal and business communication skills
  • Demonstrated ability to work in a cross functional team
  • Adheres to company and facility specific policies and procedures, including SOP, training and meeting requirements
  • Always observe safety precautions and regulations in all areas where duties are performed
  • Responsible for reporting all safety hazards and potential unsafe working conditions
  • Ensures Humacyte or other required trainings/certifications are up to date
  • Represents the organization in a positive and professional manner
  • Reports to work on time and as scheduled
  • Willingness to travel within assigned region, this may include frequent air travel

Requirements

  • MD/DO, PhD, DMSc, or NP/PA degree required
  • A minimum of 2 years of experience in a Medical Science Liaison or equivalent position required
  • Willingness to travel – 50%+
  • Preferably Midwest-based, as the territory covered will include frequent travel to Chicago, MN, Milwaukee, Michigan and other nearby states
  • Experience in vascular surgery, surgery, regenerative medicine, nephrology and/or cardiovascular medicine is preferred
  • MSL-BC is a plus

Benefits

  • Stock Options
  • 401(k) Matching
  • Medical, Dental & Vision
  • Long Term Disability
  • Short Term Disability
  • Life Insurance
  • 23 Days PTO
  • 10 Holidays + 2 Floating
  • Paid Parental Leave

Company overview

Humacyte Global Inc. (Nasdaq: HUMA) is a pioneering biotechnology company specializing in regenerative medicine and tissue engineering. Founded in 2004 and headquartered in Durham, North Carolina, the company has developed a groundbreaking bioengineering platform that creates universally implantable, acellular tissue engineered vessels (ATEV™). In December 2024, Humacyte achieved a significant milestone when the FDA granted full approval for its first product, Symvess™, an acellular tissue engineered vessel for extremity arterial trauma repair. This represents the first FDA-approved, human-derived biologic vessel for vascular injury treatment. The company's innovative platform transforms human cells into off-the-shelf regenerative tissues designed to be universally implantable and capable of remodeling with the patient's own cells over time. Humacyte's technology is being investigated for multiple clinical applications including arteriovenous access for hemodialysis, peripheral arterial disease, coronary artery bypass grafts, and treatment of type 1 diabetes. With over 215 employees, the company continues to advance its mission of engineering regenerative medicine products to save and improve patient lives through bioengineered human tissues and organs.

Explore more jobs of your matchFind more biopharma roles with GetBioJob.