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Lexeo TherapeuticsLT

Associate Director, Medical Writing and AI Implementation

Based in New York City, Lexeo Therapeutics is a clinical-stage genetic medicines company dedicated to transforming healthcare by applying pioneering science to fundamentally change how disease is treated.

Lexeo Therapeutics

Employee count: 51-200

Salary: 166k-195k USD

United States only

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The Associate Director, Medical Writing and AI Implementation will support the Medical Writing function at Lexeo, generating and managing clinical and regulatory documents, and implementing AI tools to drive optimization and efficiency. This role will be responsible for planning, development, and oversight of study and program level documents, managing medical writing and regulatory operations resources, and contributing to process improvement initiatives.

Requirements

  • Draft and contribute to the development of high-quality submission-ready documents such as protocols, protocol amendments, clinical study reports, and others.
  • Ensure the quality of deliverables by conducting editorial reviews of documents and completing or managing the quality checking of documents according to Lexeo standards.
  • Manage the document development process for deliverables, including planning aspects, project execution, and project finalization.
  • Publish documents for submission and/or oversee Regulatory Operations vendors as needed and review published documents prior to submission.
  • Use AI and automation to support publishing activities such as document formatting, hyperlinking, and validation checks.
  • Use AI capabilities and implement new AI of appropriate scope to improve efficiencies and optimize processes of all activities related to Regulatory and Medical Writing.
  • Act as the lead for training the medical writing (and regulatory and clinical development as appropriate) team(s) on new AI/digital tools and updated workflows.
  • Continuously monitor emerging trends and best practices in medical writing and AI.
  • Propose and lead process improvement initiatives that enhance document quality or team productivity.
  • Identify and implement organizational efficiencies for document development and quality, document management, and submission management.
  • Serve as a StartingPoint Administrator, managing template upgrades, internal user support, and cross-departmental training.

Benefits

  • Generous Paid Time Off
  • 401k Matching
  • Retirement Plan
  • Visa Sponsorship
  • Four Day Work Week
  • Generous Parental Leave
  • Tuition Reimbursement
  • Relocation Assistance

About the job

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Job type

Full Time

Experience level

Salary

Salary: 166k-195k USD

Location requirements

Hiring timezones

United States +/- 0 hours

About Lexeo Therapeutics

Learn more about Lexeo Therapeutics and their company culture.

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Based in New York City, Lexeo Therapeutics is a clinical-stage genetic medicines company dedicated to transforming healthcare by applying pioneering science to fundamentally change how disease is treated. Building on groundbreaking research from Weill Cornell Medicine and the University of California San Diego, Lexeo partners with preeminent institutions on the cutting edge of gene therapy research. Our approach prioritizes high-impact genetic medicine candidates for cardiovascular diseases and APOE4-associated Alzheimer’s disease. By leveraging early proof-of-concept data, we are committed to efficient development and advanced manufacturing to address the underlying genetic causes of devastating diseases.

Our pipeline includes investigational AAV-mediated gene therapies in both cardiovascular conditions and conditions of the central nervous system (CNS). We aim to create substantial positive impacts and reduce the burdens placed on patients and healthcare systems. Lexeo's management team comprises pioneers and driven leaders with decades of experience in gene therapy and rare diseases. We remain focused on employing strategic partnerships and collaborations to push the boundaries of gene therapy and offer potential cures for complex genetic disorders. With an FDA-granted Fast Track designation for our therapies, we are poised to advance clinical trials that could change the lives of the patients we serve.

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Lexeo Therapeutics

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