Description

Role Summary The Associate Director, Medical Writing will support the Medical Writing function at Lexeo, working cross-functionally to generate and manage the development of clinical and regulatory documents. This role will also take a lead in implementing artificial intelligence (AI) tools to drive optimization and efficiency in all aspects of regulatory and medical writing. This role will be responsible for the planning, development, and oversight of study and program level documents with a focus on accuracy, quality, and compliance. Additionally, the role will manage medical writing and regulatory operations resources, including vendors and partners, and contribute to process improvement initiatives.

About Lexeo

Lexeo Therapeutics is a clinical-stage genetic medicine company headquartered in New York City, pioneering cardiac genetic medicine candidates to treat the root causes of inherited cardiovascular diseases. Our lead program, LX2006, targets cardiomyopathy associated with Friedreich’s Ataxia and anchors a broader pipeline addressing genetically defined conditions such as hypertrophic and arrhythmogenic cardiomyopathies. Backed by a strong financial foundation, Lexeo is positioned to translate groundbreaking science into durable clinical impact.

Our work culture is a hybrid model with 2 days/week in the New York City office and 3 days working from home.

Lexeo Therapeutics is an EEO employer committed to an exciting, diverse, and enriching work environment.

Associate Director, Medical Writing and AI Implementation

Description

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