Medical Writer (Medical Aesthetics Training Materials)

Posted 10 July 2024
Salary US$80 - US$90 per hour
LocationLos Angeles
Job type Contract
DisciplineLife Science Recruitment
Contact NameColin Murray-Bain

Job description

Location: Remote (US)

Contract Length: 6 Months

Pay Rate: $80-90/hr

Job Description:

We're looking for a Medical Writer who lives and breathes medical aesthetics to join a newly formed in-house Curricula team. In this role, you will be writing clinical educational materials and presentations for the next generation of our offerings across live and virtual training programs.

Reporting into the Associate Director, you will work alongside creatives and curricula experts to bring clinical education to life, keeping in mind adult learning principles.

This contractor role is responsible for assisting in the development of curricula across educational programs, primarily writing and referencing content for our facial injectables medical education.

Essential Duties and Responsibilities include the following (other duties may be assigned.):

  • Technical writing for medical aesthetics training content including presentations, learning module scripts, classroom materials, etc
  • Review relevant medical literature and reference materials to fact check information and stay current on latest trends
  • Synthesize complex topics into digestible educational content, adhering to adult learning principles
  • Ensure content adheres to creative and curricula briefs, brand guidelines, and MLRC review guidelines
  • Support with Medical, Legal, Regulatory, and Compliance review systems and processes, ensuring accuracy of copy


  • Bachelor's degree is required.
  • Minimum of 5 years related experience is preferred.
  • 2+ years in a Medical Education role is favorable.
  • Proficient with Microsoft Office, including Outlook, Word, Excel and PowerPoint.
  • Excellent verbal and written communication skills, with a demonstrated ability to communicate clearly and professionally.
  • Knowledge of FDA and regulatory statutes, with the ability to function in an environment controlled by outside regulatory entities.
  • High degree of flexibility in adapting to a rapidly changing environment.
  • Occasional flexibility in work hours, including weekends, may be required.
  • Excellent interpersonal and communication skills.
  • Responsible for performing all duties in compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements

Our role in supporting diversity and inclusion
As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.