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!
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.
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
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.
Maria 已在 Certara 任职超过 26 年，最初从事监管写作和质量保证工作，后来晋升到现在的职位，即非临床/CMC 监管写作团队的负责人。
作为一名科学家和医学作家，Linda 在制药行业拥有超过 35 年的工作经验。在加入 Certara 之前，她是 Eli Lilly 的科学传播顾问，负责监督由 TPO 支持的医学出版物。
Maria 已在 Certara 任职超过 26 年，最初从事监管写作和质量保证工作，后来晋升到现在的职位，即非临床/CMC 监管写作团队的负责人。
作为一名科学家和医学作家，Linda 在制药行业拥有超过 35 年的工作经验。在加入 Certara 之前，她是 Eli Lilly 的科学传播顾问，负责监督由 TPO 支持的医学出版物。
