We’re hiring medical and regulatory writers looking for:

  • Meaningful work that provides a sense of purpose and mission
  • Remote and flexible options, including part-time, freelance and consulting opportunities
  • A collaborative environment
  • Learning and career growth opportunities

“I joined Certara for the opportunity to work at an innovative organization that is growing and evolving to meet the needs of global regulators and our clients. I love the collaborative, supportive, and flexible environment where I can work to bring meaningful solutions to patients around the globe.”

– Heather Graham, Vice President, Regulatory Writing and Scientific Publications


Certara Synchrogenix assures and accelerates the approval of and access to medical innovations through a unique combination of customized regulatory strategy, document authoring, medical communications and publications, and operations solutions.  Our proven record of success is built on our expertise and an unrivaled commitment to quality and compliance, combined with the use of advanced technologies to enhance speed and efficiency.

We have a range of Regulatory and Medical Writing opportunities available. Join us!

Principal Regulatory Writer

The Principal Regulatory Writer is a major contributor to document authorship for a variety of documents across different service lines.   The Principal Regulatory Writer is the project leader and authoring contributor for all types of client engagements, while mentoring others in the knowledge of authoring regulatory documents.

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Principal Regulatory Writer
Associate Principal Regulatory Writer

Associate Principal Regulatory Writer

Associate Principal Regulatory Writers are critical members of the regulatory services team. They do more than prepare high-quality documentation for regulatory submissions; they help streamline the regulatory documentation process and provide strategic guidance and best practices for our clients. The Associate Principal Regulatory Writer is a significant contributor to document authorship in various therapeutic areas and global markets.

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Senior Medical Writer

The Senior Medical Writer supports our clients by drafting medical publications with knowledge of publications processes and requirements. The Senior Medical Writer is a client-facing role, working collaboratively across our team, leading projects, writing publications and mentoring junior colleagues.

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Senior Medical Writer
Maria Lopez
Maria Lopez Director, Nonclinical/CMC Regulatory Writing

Maria has been at Certara for over 23 years, starting out in regulatory writing and quality assurance and advancing to her current role where she heads up the nonclinical/CMC regulatory writing team.

Certara Mari Welke
Mari Welke Director, Safety and Innovation

Mari brings nearly 25 years of industry experience, from both sponsor and service provider perspectives, spanning clinical development, project management, process improvement initiatives, medical writing, safety analysis, clinical trial disclosure, team management, and systems development.  She works with clients and internal colleagues to bring future solutions to safety documents and the transparency and disclosure space.

Linda Tabas
Linda Tabas Director, Medical Publications & Communications

Linda has over 30 years of experience in scientific communications and publishing. Prior to joining Certara, she was a scientific writing, communications consultant at Eli Lilly, overseeing medical publications supported by TPOs.

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