Our RESETTM clinical trials with rese-cel (investigational CD19-CAR T cell therapy) in lupus, myositis, systemic sclerosis, and pemphigus vulgaris are now recruiting.

Join Our Crew

Manager/Senior Manager Medical Writer, Clinical and Regulatory Medical Writing (Remote)

About the Position

Reporting to the Senior Director, Clinical and Regulatory Medical Writing, the Manager/Senior Manager Medical Writer is a key member of Regulatory Affairs. You will plan, author, and finalize clinical and regulatory documents that support Cabaletta Bio’s development programs, ensuring they are clear, accurate, and strategically aligned. You will partner with cross-functional teams, including Clinical, Biostatistics, Quality, and Regulatory to ensure documents meet US, EU, and ICH standards.

Responsibilities Include

  • Author clinical and regulatory documents for cell and gene therapy programs, including INDs, Module 2 documents supporting BLAs, protocols and amendments, investigator brochures, and clinical study reports.
  • Manage document timelines and review workflows in Veeva Vault, keeping team members informed of expectations and milestones to ensure timely reviews and approvals.
  • Perform quality control and editorial review to ensure documents meet standards for accuracy, consistency, structure, and clarity.
  • Prepare documents for submission, including publishing readiness, quality checks, and finalization of supporting literature.
  • Maintain high quality and efficiency in technical documentation that supports regulatory filings.
  • Mentor junior medical writers and subject matter experts on technical writing skills and best practices.
  • Participate in project team meetings and offer proactive solutions and advice.
  • Complete training on company document management systems, and author or review departmental (clinical and regulatory) SOPs as needed.
  • Perform other duties as assigned.

Required Qualifications

  • Bachelors or masters degree in biological sciences; with 6 years’ experience or Ph.D. and 2 years’ experience in a technical writing capacity.
  • Familiarity with the key requirements for regulatory submissions in ICH regions as stipulated in applicable regulations and guidelines for pharmaceuticals/biologics.
  • Experience in reviewing and writing regulatory submission documents for global regulatory filings such as IMPD, INDs, MAAs, NDAs, and BLAs, is preferred.
  • Ability to critically analyze, synthesize, and present complex information in well-constructed documents.
  • Working knowledge of drug/biologics development, clinical research, study design, biostatistics, the regulatory environment, and medical terminology.
  • Confidence to present to management, peers, and scientific or business collaborators.
  • Ability to support multiple projects and to prioritize work independently.
  • Ability to comply with company and/or industry style guides and templates.
  • Ability to guide and train others in the writing of technical documentation.
  • Fluent with written and spoken English with excellent attention to detail relative to consistency, grammar, syntax, and scientific accuracy.
  • Advanced MS Skills in Word, Excel, and Adobe Pro.
  • Strong team orientation and passion for continuous self-development.
  • Experience in the biotech industry or in a startup industrial setting is preferred.


Apply For This Job

How to Apply

Please click the link at the bottom of the posting to submit an application.

Benefits

Our most important asset is our people and we offer competitive benefits including health and retirement, PTO, and stock option plans.

Equal Opportunity Employer

Cabaletta Bio is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability, protected veteran status or any other basis protected by applicable law.