Medical writer

• Write and edit clinical regulatory documents for clarity, and accuracy according to defined sponsor standards
• Work with lead writer and project team to develop document messages and data presentations within submission timelines to meet company objectives
• Provide writing support for a wide range of documents, including but not limited to investigator’s brochures, clinical study protocols and reports, integrated summaries, literature reviews, and SOPs
• Ensure that documents comply with International Conference on Harmonisation guidelines, SOPs, and Good Clinical Practices

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