Regenerative Medicine Coordinator

6 days ago


Irvine, California, United States Avita Medical Full time
Job Summary

AVITA Medical is a leading regenerative medicine company seeking a highly skilled Medical Affairs Associate to join our team. As a key contributor to our Medical Affairs Department, you will be responsible for assisting in the development and maintenance of medical information and communications.

Key Responsibilities
  • Data Analysis and Medical Writing Support: Provide data analysis and medical writing support to internal and external stakeholders, ensuring the creation of fair and scientifically balanced materials.
  • Abstract Development and Submission: Work closely with our Medical Science Liaison (MSL) team to assist in the development and submission of abstracts, showcasing our company's expertise in regenerative medicine.
  • Clinical Study and Presentation Development: Assist in the development of clinical study, abstract, and training presentations, highlighting the benefits of our innovative technologies.
  • Post-Market Surveillance: Lead medical affairs activities for post-market surveillance, ensuring compliance with regulatory requirements and maintaining the highest standards of quality.
  • Document Management: Maintain internal documents, including a bibliography and medical communication strategy, to ensure seamless communication across teams.
  • Customer Support: Support responses to healthcare professional, consumer, and investor product/medical inquiries, providing accurate and timely information.
Requirements
  • Travel: Up to 15% or as needed, to attend conferences, meetings, and other business-related events.
  • Education: Advanced degree in a medical field, life sciences, or public health preferred, with a strong foundation in medical writing and communication.
  • Communication Skills: Excellent written and oral communication skills, with the ability to effectively convey complex information to various audiences.
  • Technical Skills: Advanced knowledge of Microsoft Word, PowerPoint, and Excel, with the ability to create engaging and informative presentations.
  • Medical Communication Strategy: Understanding of medical communication strategy and its application in a regulatory environment.
  • Teamwork and Project Management: Ability to work independently and as a member of a team, with strong project management skills and attention to detail.
  • Medical Writing: Experience in medical writing, including study protocols, data analysis, abstracts, posters, manuscripts, and presentations.
  • Post-Market Surveillance: Knowledge of post-market surveillance programs for regulatory bodies and the ability to manage these programs effectively.

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