Principal Medical Writer Associate Director

Job Title: Principal Medical Writer Associate Director

Location: USA, Remote. Proximity to Cambridge/Boston, MA or Morristown, NJ is highly desirable for attending occasional team meetings

About the Job

Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress.

Global Medical writing and Document management serves to generate timely, high quality, cost effective and regulatory compliant documents. Our mission is to synergize and harness evolving technologies pushing the edge of regulatory writing.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Main Responsibilities:

Document Development

Create high-quality regulatory-compliant clinical documents supporting product life cycle

Ensure timely delivery while maintaining compliance with standards

Innovation

Lead implementation of new digital technologies and AI solutions

Drive process improvements for efficiency gains

Regulatory Expertise

Prepare registration dossiers and Health Authority responses

Monitor and implement regulatory documentation requirements

Project Management

Lead cross-functional initiatives as Subject Matter Expert

Drive change management within writing teams

Communication

Update relevant stakeholders on project progress and needs

Maintain accurate information in planning, tracking, and reporting toolsEnsure consistent communication across ClinDoc functions

Coordination

Mentor junior writers and review contract work

Quality & Training

Develop training programs and documentation standards

Build effective relationships with stakeholders and partners…

About You

Core Experience:

Six+ years as medical writer or equivalent specialist role

Proven track record leading multiple clinical documentation projects

Expert in clinical documentation preparation

Clinical Development Knowledge:

Demonstrated expertise in clinical development processes

Strong understanding of clinical study methodology and basic statistics

Knowledge of regulatory environment

Proficient in document management systems and authoring platforms

Professional Attributes:

Strong attention to detail and deadline management

Excellent organizational and follow-up abilities

Proven ability to work independently and in global teams

Technical skills:

Expertise in electronic document management and Microsoft Office

Proven experience in implementing emerging innovative digital technologies, including content reuse strategies and AI-assisted document authoring solutions.

Why Choose Us?

Bring the miracles of science to life alongside a supportive, future-focused team.

Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.

Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.

Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

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All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.

Full Time