Senior Regulatory Medical Writer: Lead Clinical Submissions - Montreal (administrative region) - Fortrea

Description

A global pharmaceutical company in Montreal is seeking a Senior Regulatory Medical Writer to lead the development of clinical regulatory documents.

Ideal candidates should have at least 4 years of regulatory medical writing experience and a Bachelor's degree in life sciences.

Responsibilities include coordinating cross-functional teams and developing high-complexity regulatory submissions. This position offers opportunities for career growth in a collaborative environment.
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