Medical Science Liaison

H
HumacyteBiotechnology, medical affairs
Source API remote eligibility restrictions: United StatesFull-TimeMiddle
Salary not disclosed
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Job Details

Languages
Able to communicate effectively in English, both verbally and in writing
Experience
A minimum of 2 years of experience in a Medical Science Liaison or equivalent position required
Required Skills
Microsoft Office

Requirements

  • MD/DO, PhD, DMSc, or NP/PA degree required.
  • At least 2 years of experience in a Medical Science Liaison or equivalent position required.
  • Willingness to travel 50%+.
  • Experience in vascular surgery, surgery, regenerative medicine, nephrology, or cardiovascular medicine preferred.
  • MSL-BC certification is a plus.
  • Able to communicate effectively in English, verbally and in writing.
  • Demonstrated communication and influencing skills.
  • Demonstrated ability to build strong relationships and work in cross-functional teams.
  • Strong presentation and training skills.
  • Basic computer skills, including MS Word, Excel, PowerPoint, and Outlook.

Responsibilities

  • Engage external stakeholders and communicate scientific and clinical information about Humacyte products.
  • Develop a network of Key Opinion Leaders and KOL engagement strategies using medical and scientific data.
  • Execute territory plans aligned with Medical Affairs plans.
  • Identify and communicate clinical and research insights from KOLs to appropriate departments.
  • Collaborate with the clinical team to identify investigators and educate investigators and sites.
  • Provide scientific support and medical education to healthcare professionals through presentations and meetings.
  • Collaborate on educational and medical/scientific materials for conferences and KOL engagement activities.
  • Review written and electronic materials, including clinical trial protocols, study tools, and clinical study reports, for accuracy and regulatory compliance.
  • Work with CRO clinical research associates to ensure investigators and site staff understand the investigational product, protocol eligibility criteria, and study procedures.
  • Provide detailed reports of external stakeholder interactions and keep abreast of relevant research and developments.
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