Medical Writer
7 days ago
We are seeking a highly skilled Regulatory Technical Writer to join our team at Lifelancer, a leading talent-hiring platform in Life Sciences, Pharma, and IT. As a Regulatory Technical Writer, you will play a key role in supporting the Regulatory Affairs department in developing the global evidence base for company development programs.
In this role, you will be responsible for preparing, writing, editing, and reviewing high-quality regulatory documents founded in regulation and supported by science for submission to regulatory agencies and health authorities. You will work closely with the Global Regulatory Affairs (GRA) team to ensure that all regulatory submissions are accurate, complete, and compliant with regulatory requirements.
This is a great opportunity to work with a talented team of professionals in the Life Sciences industry and to develop your skills and expertise in regulatory affairs. If you are passionate about medical writing and want to make a real difference in the lives of patients, please apply for this position.
Estimated Salary Range: $93,500 - $133,600
Responsibilities:- Prepare, write, edit, and review high-quality regulatory documents founded in regulation and supported by science for submission to regulatory agencies and health authorities.
- Provide support for the preparation and submission of critical regulatory documents and responses to health authority information requests using available reference materials, scientific literature, and content provided by the Global Regulatory Affairs (GRA) team members functional area contributors.
- Collaborate with project teams and functional area contributors to advance global regulatory programs and product development projects.
- Assist with the coordination of the review, approval, QC, and other activities involved in the production of regulatory documents.
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