MEDICAL WRITER - MEDICAL DEVICES (M/F/D)
Descrição da oferta de emprego
Your new role This professional will be responsible for evaluate and analyses clinical evidence, lead CER projects, create and maintain clinical documents, collaborate with teams, ensure data integrity and regulatory compliance, and contribute 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 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 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.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.
#LI-DNI # - Joana Ganhao
Detalhes da oferta
- Hays
- Em todo Portugal
- Indeterminado - Indeterminado
- Indeterminado
- 13/12/2024
- 13/03/2025
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