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In addition to regulatory writing, the Regulatory Medical Writer II will also assist in the coordination, assembly, writing, editing and quality control of study/data reports, and/or protocols, which accurately reflect the study data and fulfill all protocol and regulatory requirements. The Regulatory Medical Writer II is an entry-level professional responsible for drafting, editing, and formatting early-stage regulatory submission documents for both pharmaceutical drugs (INDs) and medical devices (510k applications).

YEAR

CBSET, Inc. is a recognized leader in preclinical biomedical research. We make it our mission to help our sponsors accelerate the development of novel and innovative pharmaceuticals, biotechnologies, and medical devices. CBSET offers extensive regulatory and scientific expertise to the medtech and biopharma industry around the globe in order to rapidly transform early-stage concepts into novel therapies.

Author Jobs in Cambridge, MA

Regulatory Medical Writer II CBSET Inc

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