We are seeking a Regulatory Affairs professional to support with development activities for large molecules for a globally known Biotech.
Due to the size of the company, you will be involved in career enhancing projects and gain exposure usually reserved for more senior roles.
Working alongside a GRL, you will support on RA strategy development and execution, for both early and late stage development projects (large molecule). You will support with HA interactions globally, whilst advising other departments and project teams on current regulations related to the pipeline projects.
This role is offered on a permanent remote basis.
• Minimum 3-7 years RA experience
• Experience with EMA or FDA
• Large molecule expertise with development projects
• Works well under pressure
• A team player