Senior PV Medical Writer & Mentor

Ergomed; España; On-site; EUR 42,000 - 65,000; Full time

Job summary

Ergomed is seeking an experienced pharmacovigilance medical writer to join our growing medical writing team. You will deliver high-quality regulatory documents, strengthen client relationships, and support the growth of the wider team.

Ideal candidates have an MD, pharmacy or life science degree with at least two years in medical writing within a CRO; you will train junior writers, ensure scientific accuracy, and help implement quality standards across projects.

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.

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.

Skills

Medical writing

Regulatory writing

Mentoring

English fluency

Education

MD/Pharmacy/Life Science degree

Masters/PhD desirable

Job description

Ergomed is seeking an experienced pharmacovigilance medical writer to join our growing medical writing team. You will deliver high-quality regulatory documents, strengthen client relationships, and support the growth of the wider team.

Ideal candidates have an MD, pharmacy or life science degree with at least two years in medical writing within a CRO; you will train junior writers, ensure scientific accuracy, and help implement quality standards across projects.