Senior Medical Writer

Barrington James; Paris; Sur place; EUR 50 000 - 70 000; Plein temps

Résumé du poste

A fast-growing global AI company is looking for an experienced Medical Writer to join their team in Paris. This role involves developing regulatory documents and ensuring compliance with global standards through the utilization of AI and automation. Candidates should have over 5 years of experience in medical writing, particularly in pharmacovigilance, with strong attention to detail and communication skills. This is an exciting opportunity to integrate cutting-edge technology within the medical writing field.

Qualifications

• 5+ years of experience in medical writing, specifically with pharmacovigilance documents.
• Strong knowledge of PV regulations and clinical documents.
• Familiarity with document automation and AI-driven content is advantageous.

Responsabilités

• Develop and maintain templates for automated regulatory documents.
• Review AI-generated safety reports for compliance and accuracy.
• Collaborate with teams to enhance workflows.
• Ensure documents meet global regulatory standards.
• Stay updated with industry trends to support automation improvements.

Connaissances

Medical writing

Pharmacovigilance knowledge

Attention to detail

Communication skills

Collaboration skills

Description du poste

A fast-growing global AI company is seeking an experienced Medical Writer with a background in pharmacovigilance to join their innovative team. This hands-on role focuses on leveraging AI and automation to streamline regulatory document creation while maintaining the highest quality standards.

Key Responsibilities

• Develop and maintain templates and content models for automated regulatory documents
• Review and validate AI-generated safety reports for accuracy and compliance
• Collaborate with product, engineering, and regulatory teams to improve workflows
• Ensure outputs meet global regulatory standards (FDA, EMA, ICH, and others)
• Keep up-to-date with industry trends and regulatory updates to support automation improvements

Requirements

• 5+ years of experience in medical writing, with a focus on pharmacovigilance documents
• Strong knowledge of PV regulations, clinical documents, and safety databases
• Experience with structured data, document automation, or AI-driven content is a plus
• Excellent attention to detail, communication, and collaboration skills
• Ability to manage multiple projects and meet deadlines in a fast-paced environment

This is a unique opportunity to combine medical writing expertise with cutting-edge AI technology, helping transform regulatory document workflows globally.

If you’re interested in learning more, feel free to reach out or apply below :

✉ [e-mail]

☎ [phone]