# Associate Director, Medical Writing at Latigo Biotherapeutics

- Company: Latigo Biotherapeutics
- What the company does: Backed by 5AM Ventures.
- Company website: https://latigobio.com
- Type: Startups
- Level: Principal and up
- Location: Thousand Oaks, California
- Work setup: On-site
- Pay: $200K to $220K base salary per year (USD)
- Posted: 2026-09-01
- Apply by: 2026-10-16
- Apply: https://latigobio.bamboohr.com/careers/60
- Page: https://www.1752.vc/careers/jobs/latigo-biotherapeutics-associate-director-medical-writing/

## About the role

Latigo is seeking an experienced and highly motivated Associate Director, Medical Writing to join our Clinical Development organization. This hands-on role will be responsible for authoring and managing key clinical and regulatory documents, with a primary focus on clinical study protocols, protocol amendments, and clinical study reports (CSRs) supporting our growing development portfolio.

## What they're looking for

- Author, review, and manage clinical development and regulatory documents, including protocols, protocol amendments, CSRs, investigator brochures, briefing documents, and clinical sections of regulatory submissions
- Lead document planning, development, review cycles, and comment resolution to ensure on-time, high-quality deliverables
- Collaborate with cross-functional teams to interpret and communicate complex scientific, clinical, statistical, and pharmacology data
- Develop and maintain templates, style guides, document standards, and best practices to support high-quality and efficient document production
- Ensure compliance with FDA regulations, ICH guidelines, GCP, and other applicable regulatory requirements
- Contribute to INDs and other global regulatory submissions, including regulatory responses and supporting documentation

Tags: Clinical Development