Are you an experienced regulatory affairs writer looking for a new challenge? We have just the opportunity for you! Our client, a top medical devices company, is seeking a Senior Regulatory Affairs Writer to join their dynamic team. This role offers a stimulating work environment at the forefront of medical research, along with ample opportunities for professional growth and development. And the best part? It’s fully remote, allowing you to work from anywhere in the UK, Israel, or Germany.

Responsibilities:

– Write and/or edit various clinical regulatory documents: As a Senior Regulatory Affairs Writer, you will be responsible for writing and editing a wide range of clinical regulatory documents, including CSRs, IBs, Protocols, Summaries, Briefing Books, Pediatric Plans, and Model 2 summaries for submissions. Your expertise in driving project consensus and foreseeing potential issues will be highly valued
– Oversee and mentor: Take on a leadership role and ove...