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Associate Medical Writer
hace 4 semanas
**Job Description**:
**Primary Responsibilities**:
- Prepares selected components of regulatory clinical documentation
- Develops knowledge of regulatory medical writing and therapeutic area/investigational product to support pipeline projects
- Participates, with supervision, on document-specific teams
- Develops competence in writing, editing, and reviewing clinical study reports, patient narratives, investigator brochures, and other clinical regulatory documents per company and other guidelines
- Acquires a thorough comprehension of medical writing tasks, including the design, planning, and preparation of clinical documentation in support of clinical development, trials, and sections of filings
- Identifies challenges associated with medical writing scope of work, seeks advice from management and others as needed, and exercises negotiation and communication skills with project team members
- May participate in initiatives to improve medical writing processes and standards
**Education Minimum Requirements**:
- Degree in a life science, preferably related to pharmacy or medicine Bachelor’s degree with 2+ years; MS with 1+ year; or doctoral-level degree (e.g., PhD, MD, DVM, DO, PharmD) with
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