Medical Writer III

Job Summary

Seeking a detail-oriented and motivated Medical Writer III in pharmacovigilance, this full-time remote position will author and review regulatory documents, ensure compliance and accuracy, and foster client relationships while mentoring junior writers.

Key Responsibilities:

• Author, review, and quality check regulatory and pharmacovigilance documents such as PSURs, PADERs, and Risk Management Plans
• Ensure scientific accuracy and regulatory compliance of documents, delivering them within agreed timelines
• Collaborate with cross-functional teams to analyze and present safety data, while mentoring junior medical writers

Required Qualifications:

• MD, pharmacy, or Life Science degree; a Masters or PhD is desirable
• Minimum 2 years of experience in Medical Writing and related fields, preferably within a CRO environment
• Proven ability to manage multiple tasks and prioritize workload effectively
• Experience in training and mentoring Associate Medical Writers
• Fluency in English; proficiency in an additional language is a benefit