Job Description

We are looking for an experienced pharmacovigilance medical writer to join our growing medical writing team.

What We're Looking For: A highly motivated and detail-oriented medical writer who combines strong regulatory writing expertise with a client-focused mindset and a passion for developing others. You will play a key role in delivering high-quality regulatory documents, strengthening client relationships, and supporting the growth of the wider team. The Medical Writer will be responsible for medical writing including:

Key Responsibilities:

- Author, review, and quality check a range of regulatory and pharmacovigilance documents, including:
- PSURs/PBRERs
- PADERs
- ACOs
- DSURs
- Risk Management Plans (RMPs)

- Ensure documents are scientifically accurate,



regulatory compliant, and delivered within agreed timelines.
- Collaborate with cross-functional teams to analyse, interpret, and present safety data effectively.
- Act as a trusted point of contact for clients, supporting project delivery and fostering strong working relationships.
- Provide guidance, mentoring, and knowledge sharing to junior medical writers to support their professional growth and development.
- Contribute to process improvements and the continuous enhancement of medical writing quality standards.

📌 Medical Writer III (Pharmacovigilance) (Madrid)
🏢 Primevigilance
📍 Madrid