Medical Writer III (Pharmacovigilance)
- 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, compliant and delivered on time
- Collaborate with cross-functional teams to analyse and present safety data
- 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 associated fields such as case processing, signal detection or risk management
- Experience within a CRO environment preferred
- Ability to manage multiple tasks with attention to detail
- Strong team player
- Fluent English
Benefits
- Global, collaborative culture focused on kindness, flexibility and growth
About the Company
Ergomed is a global pharmacovigilance and clinical research specialist focused on patient safety.
Listed via Career sites