Medical Writer

Job Summary

A company is looking for a Medical Writer to develop regulatory-compliant clinical documents and support innovative digital solutions.

Key Responsibilities

• Create high-quality regulatory-compliant clinical documents supporting product lifecycle
• Support implementation of new digital technologies and AI solutions
• Prepare clinical documents for registration dossiers and maintain awareness of regulatory requirements

Required Qualifications

• Must be currently enrolled in the 2024-2026 Rutgers Sanofi PharmD Fellows Program
• Minimum 1 year as a medical writer or equivalent experience in Clinical Research
• Experience in preparing clinical documents and regulatory submissions
• Basic understanding of clinical development processes and clinical study methodology
• Familiarity with the regulatory environment and medical terminology