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Service writer • midland tx
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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