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: Author, review, and quality check a range of regulatory and pharmacovigilance documents, including: 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.

Qualifications MD, pharmacy or Life Science degree (Masters or PhD is desirable) Minimum 2 years' experience in Medical Writing and associated fields (case processing, signal detection or risk management) ideally within a CRO environment Ability to manage multiple and varied tasks and prioritize workload with attention to detail Ability to effectively train and mentor Associate Medical Writers Must be a strong team player Fluency in English, an additional language is a benefit Additional Information When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You'll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.

Quality: we hold ourselves to the standard patients deserve.

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