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, 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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