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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.

Certara Synchrogenix Stats

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

Senior Regulatory Writer

The Senior Regulatory Writer (SRW) is a major contributor to document authorship for a variety of documents across different service lines. The SRW will be the project lead on smaller projects, interfacing directly with the client, but also support larger, more complex engagements as a member of a larger delivery team.

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Senior Regulatory Writer
Associate Principal Regulatory Writer - Clinical

Associate Principal Regulatory Writer - Clinical

Regulatory Writers prepare high quality documentation for regulatory submissions in order to help streamline the regulatory approval process for our clients. The APRW will work closely with client and internal and partner organization teams to lead development of strategies for organizing and preparing regulatory documents

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Associate Principal Regulatory Writer - Non Clinical

The Associate Principal Regulatory Writer (APRW) is a major contributor to document authorship for a variety of nonclinical documents across different therapeutic areas. The APRW will be the project lead on smaller projects, interfacing directly with the client, but also support larger, more complex engagements as a member of a larger delivery team.

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Associate Principal Regulatory Writer - Non Clinical
Maria Lopez
Maria Lopez Director, Nonclinical/CMC Regulatory Writing

Maria has been at Certara for over 26 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.

Linda Tabas
Linda Tabas, ISMPP CMPP™ Director, Medical Publications & Communications

Linda has over 35 years of experience in the pharmaceutical industry as a scientist and medical writer. Prior to joining Certara, she was a scientific communications consultant at Eli Lilly, overseeing medical publications supported by TPOs.