The Associate Director, Medical Writing will be responsible for writing and coordinating the writing of various clinical and regulatory documents, including protocols/amendments, investigator brochures, clinical study reports, and NDA/BLA submission documents. The Associate Director, Medical Writing will work closely with cross-functional teams to manage the preparation of written clinical and regulatory documents, ensuring that they are of high quality.
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USD/year
This critical role will ensure the medical integrity, topicality and timeliness of the content for client projects and help ensure compliance across Medical and Legal.The Medical Director is responsible for providing medical expertise to clients and internal teams while leading strategy and developing medical content.