Medical Writing Manager

A company is looking for a Medical Writing Manager to prepare and review clinical and regulatory documents in support of drug development. Key Responsibilities Lead the authoring process for various clinical and regulatory documents Represent Medical Writing on project teams and provide subject matter expertise Research and implement best authoring practices while training team members Required Qualifications BS / BA in life sciences or related field with 6+ years of medical writing experience, or a Master's degree with 4+ years, or a PhD with 2+ years of relevant experience Experience leading NDA / MAA submissions or authoring key supporting documents is preferred Strong understanding of the medical writing process and regulatory requirements Ability to independently interpret and communicate scientific data Experience working with and leading contract medical writers