Medical Writer - Medical Devices (M/F/D)

Your new company
Join a multinational medical devices pharmaceutical company assuming Medical Writer, based in Lisbon.

Your new role
This professional will be responsible for evaluating and analyzing clinical evidence, leading CER projects, creating and maintaining clinical documents, collaborating with teams, ensuring data integrity and regulatory compliance, and contributing to regulatory submissions. You will work frequently with Regulatory Affairs, Marketing, project teams, and NPD project managers, as well as with external clinicians.

What you'll need to succeed
We are looking for a professional with at least 5 years' experience in medical writing or clinical affairs in the medical devices industry. You should have an academic background and experience in the pharmaceutical industry. Strong communication skills, both oral and written, in English are essential.

What you'll get in return
This is an excellent opportunity to join a multinational pharmaceutical company, with attractive benefits and a good work environment.

What you need to know
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV.

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