Associate Director, Medical Writing and AI Implementation
Full-timeEntryRegulatory Affairs
$166K - $195K/yr(from employer)
Description
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<p><span data-contrast="auto">Role Summary</span><span data-ccp-props="{"201341983":0,"335559740":257}"> </span></p>
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<p><span data-contrast="auto">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.</span><span data-ccp-props="{"201341983":0,"335559740":257}"> </span></p>
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Lexeo Therapeutics
BIOTECHNOLOGY
Gene Therapy
LocationNY - New York
Open Jobs7
Gene Therapy
View Company ProfilePipeline
A Study to Assess Real-world Patient Characteristics and Clinical Course for Symptomatic Patients WiN/A
Long-term Follow-up Study of Gene Therapy for Arrhythmogenic Cardiomyopathy Due to a Plakophilin-2 PN/A
Clinical Course Of Disease In Participants With FA-CMN/A
LX1001Phase 1
LX1001Phase 1/2