Medical Writer III (Pharmacovigilance)

Responsibilities

• Author, review and quality check PSURs/PBRERs, PADERs, ACOs, DSURs and Risk Management Plans

• Ensure documents are scientifically accurate, compliant and delivered on time

• Analyse, interpret and present safety data with cross-functional teams

• Act as a trusted point of contact for clients

• Mentor and train junior medical writers

• Contribute to process improvements and writing quality standards

Requirements

• MD, pharmacy or life science degree (Masters or PhD desirable)

• Minimum 2 years in medical writing or related pharmacovigilance fields

• Experience in case processing, signal detection or risk management, ideally in a CRO

• Ability to manage multiple tasks with attention to detail

• Strong team player

• Fluent English

Preferred Qualifications

• Additional language skills

About the Company

Ergomed is a global pharmacovigilance and clinical research provider focused on patient safety. Its values emphasize quality, integrity, agility and belonging.