Madrigal Pharmaceuticals is hiring: Senior Manager, Medical Writing in Boston

Associate Director, Medical Writing

Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction‑associated steatohepatitis (MASH). Their medication Rezdiffra is the first and only FDA‑ and European Commission‑approved treatment for MASH with moderate to advanced fibrosis.

Overview

The Associate Director of Medical Writing will ensure accuracy, consistency, and quality of clinical documents supporting our mission to develop transformative therapies for patients with MASH.

Seniorities and Employment Type

Mid‑Senior level | Full‑time | Health Care Provider | Pharmaceutical Manufacturing

Responsibilities

• Write documents supporting Phase 1 through IV clinical trials (clinical study protocols, clinical study reports, investigator brochures).
• Collaborate with cross‑functional teams to create documents that support program goals and timelines.
• Ensure documents are of the highest quality and compliant with global regulatory requirements and industry best practices.
• Contribute to updates of standard operating procedures to reflect evolving requirements.
• Develop and implement processes and systems to optimize document development efficiency and productivity.
• Stay current with regulatory guidelines, industry trends, and best practices in medical writing.

Qualifications

• 6+ years of clinical or regulatory medical writing experience supporting pharmaceutical drug development.
• Able to:
  • Analyze and interpret complex clinical data and scientific information to write clear, concise documents for a variety of audiences.
  • Ensure accuracy and consistency in the quality control of documents with precise attention to detail.
  • Work collaboratively in a fast‑paced environment while balancing multiple documents of varying complexity.
• Strong understanding of the drug development process, including clinical research, regulatory requirements and publication strategies.
• Experienced in using industry‑standard technical tools (templates, Microsoft Word macros) and electronic document management systems.
• Committed to adhere to ethical principles and industry standards, including GCP and GDP.
• Preferred:
  • Familiarity with designing and operationalizing clinical studies.
  • Advanced degree in a scientific area.
  • Experience in liver, cardiovascular or metabolic diseases.

Compensation & Benefits

Base salary range: $173,000 – $211,000 per year. All full‑time employees receive equity and are eligible for comprehensive benefits, including flexible paid time off, medical, dental, vision, life/disability insurance, 401(k) (traditional, Roth, employer match) and additional voluntary benefits such as supplemental life insurance, legal services and other offerings.

EEO & Equal Opportunity

Madrigal is an Equal Opportunity Employer. All employment is decided on the basis of qualifications, merit, and business need. Applicants will receive consideration without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, age, disability, protected veteran or disabled status, or any other characteristic protected by applicable federal, state, or local law. We are committed to providing reasonable accommodations for individuals with disabilities throughout the hiring process.

Fraud Notice

We have received reports of individuals misrepresenting themselves as Madrigal hiring managers. Any correspondence regarding employment will come from an authorized madrigalpharma.com email address or a trusted search firm partner. Do not respond to unsolicited offers, do not open attachments, and do not click links from suspicious emails. For questions regarding legitimacy, contact HR@madrigalpharma.com.

Application

Applications are being accepted on an ongoing basis and can be submitted through our Careers site.