Job Description
Fortrea is seeking an experienced Senior Regulatory Medical Writer to lead authoring and development of high-complexity clinical regulatory documents for strategic projects with global reach.
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You will own the end-to-end medical writing process from planning and cross-functional coordination through drafting, review and delivery, ensuring alignment with objectives and timelines. xqbhyrx
The role involves authoring study-level documents (protocols, SI/ICF, CSR lay summaries, IBs, regulatory packages) and
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Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.
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