Consultant Medical Writer (Drug Safety / Pharmacovigilance)
Contract | Variable Hours (Approx. 15–40 hours/week)
Overview
We are seeking an experienced Consultant Medical Writer
to support our Drug Safety and Pharmacovigilance (PV) function. This role focuses on the development of safety- and PV-related documents and content, working closely with cross-functional teams to ensure high-quality, accurate deliverables.
This is a flexible, contract-based role with variable hours, typically ranging from 15 to 40 hours per week.
Key Responsibilities
- Author and contribute to drug safety and pharmacovigilance documentation, including safety sections of regulatory and non-regulatory documents
- Collaborate with Drug Safety/PV teams to interpret and present safety data clearly and accurately
- Support the preparation of safety narratives, reports, and other PV-related materials
- Ensure consistency, scientific accuracy, and clarity across all written deliverables
- Adhere to internal standards, timelines, and quality expectations
Ideal Candidate Profile
- Background in Pharmacovigilance, Drug Safety, or Pharmacokinetics (PK/PV)
- Experience in medical writing with a focus on safety content, either in-house or as an independent consultant
- May come from a Drug Safety/PV operational role with strong writing expertise and interest
- Prior experience specifically in regulatory document writing (e.g., protocols, IBs, CSRs) is not required
Skills & Competencies
- Strong scientific writing and data interpretation skills, particularly in safety contexts
- High attention to detail and ability to communicate complex information clearly
- Reliable, responsive, and able to work independently in a remote/consulting environment
- Effective communicator with collaborative mindset
Technical & Logistical Requirements
- Access to a Windows-based laptop and familiarity with Microsoft Office tools
- Comfortable using standard business and document management systems
- Ability to integrate into an existing team structure and workflows
Additional Notes
- This role follows the same structure and expectations as other consultant medical writers within the organization
- Successful candidates will demonstrate performance aligned with high-performing peers in similar writing roles
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