Develop high quality, scientifically accurate content across a range of projects that aligns with client objectives and meets budgetary and schedule requirements
Ensure content adheres to legal and regulatory requirements (e.g. ABPI, EFPIA), and internal and external SOPs
Clear and proactive communication to ensure key information about projects is available in a timely manner
Degree level or higher in a life science, with at least 18 months’ medical education agency experience, including strong evidence of teamwork and ability to work in a high-pressure environment
Top quality scientific writing, with skills to adapt content and style to suit different audiences, plus strong project management and organisational skills
Solid understanding of the process of drug development and the regulations that drive this in the US and EU
Highly competitive package
First-class training and development
Opportunity to work on a variety of project types and therapy areas
Candidates must have the right to work in the UK BREAK
