Pharmacovigilance Medical Writer I/II - Remote

Overview

We are looking for a pharmacovigilance medical writer to join our team at PrimeVigilance, responsible for various medical writing tasks and supporting project managers.

In Short

• Responsible for writing PSURs, PBRERs, and other regulatory documents.
• Quality control of written outputs from the operations team.
• Support project managers in scheduling reports.
• Identify areas for improvement in documentation processes.
• Attend client kick-off meetings and audits.
• Provide training on aggregate report writing.
• Work collaboratively with a diverse team.
• Emphasize personal and professional growth.
• Fluency in English required; additional languages are a plus.
• Strong background in Pharmacovigilance is essential.

Requirements

• MD, pharmacy or Life Science degree (Masters or PhD preferred).
• Experience in Pharmacovigilance within a CRO environment.
• Ability to manage multiple tasks with attention to detail.
• Strong mentoring and training skills.
• Team player with a collaborative mindset.

Benefits

• Training and career development opportunities.
• Supportive working environment.
• Opportunity to work with global colleagues.
• Focus on diversity, equity, and inclusion.