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Medical Writer III (Pharmacovigilance)

Ergomed Group · Lisbon, Portugal

Writing types
Regulatory
Seniority
Entry

About the role

Responsibilities

  • Author, review and quality check PSURs/PBRERs, PADERs, ACOs, DSURs and Risk Management Plans
  • Ensure documents are scientifically accurate, regulatory compliant and delivered on time
  • Collaborate with cross-functional teams to analyse, interpret and present safety data
  • Act as a trusted point of contact for clients and support project delivery
  • Mentor and train junior medical writers
  • Contribute to process improvements and medical writing quality standards

Requirements

  • MD, pharmacy or life science degree
  • Minimum 2 years' experience in medical writing or associated fields such as case processing, signal detection or risk management
  • Ability to manage multiple tasks with attention to detail
  • Strong team player
  • Fluent English

Preferred Qualifications

  • Masters or PhD
  • Experience within a CRO environment
  • Additional language skills

About the Company

Ergomed is a global pharmaceutical services group offering clinical research, pharmacovigilance and quality consulting. Its values include quality, integrity, agility and belonging.

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