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Associate Medical Writer
hace 3 semanas
The Associate Medical Writer gains experience writing documents that support the clinical regulatory writing portfolio. With oversight, the Associate Medical Writer:
- Prepares selected components of regulatory clinical documents (e.g., clinical study reports, participant narratives, investigator’s brochure updates, informed consents) per company and regulatory requirements.
- Acquires an understanding of medical writing responsibilities, including document planning and authoring, and interpretation of data.
- Participates on document-specific teams and gains an understanding of the medical writer’s role in leading the team and the project.
- Develops knowledge of clinical development, relevant regulations, disease areas, and company products.
- Exhibits a willingness to speak up when encountering challenges across the medical writing scope of work (e.g., documents, processes, tools) in a project team environment.
- Develops competence in medical writing-specific tools and technology platforms.
- May participate in initiatives to improve medical writing processes and standards.
Qualifications, Skills, & Experience
- Degree in a scientific discipline (e.g., life sciences, pharmacy, medicine)
- Bachelor’s degree with 2+ years, master’s degree with 1+ year, or doctorate degree with
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