At a Glance
- Tasks: Create and manage technical documents for regulatory submissions in a remote setting.
- Company: MMS Holdings Inc., a leader in regulatory writing with a focus on innovation.
- Benefits: Flexible remote work, competitive salary, and opportunities for professional growth.
- Other info: Work independently while leading projects in a supportive environment.
- Why this job: Join a dynamic team and make a significant impact in the regulatory field.
- Qualifications: Experience in regulatory writing and strong collaboration skills required.
The predicted salary is between 54000 - 66000 £ per year.
MMS Holdings Inc. in the United Kingdom is seeking a skilled regulatory writer to develop, write, and manage highly technical nonclinical documents for eCTD submissions (Module 2.4/2.6), IBs, Nonclinical Study Reports, and briefing documents.
This full-time remote role requires leading projects with minimal oversight, aligning documents with regulatory guidelines, and collaborating with cross-functional teams across pharmacology, toxicology, and regulatory operations.
Senior Nonclinical Writer — Remote UK employer: MMS Holdings Inc
MMS is an exceptional employer that values innovation and collaboration, making it a fantastic place for professionals in the field of operational efficiency and technology innovation. With a strong commitment to employee growth and a supportive work culture, MMS offers unique opportunities to engage with cutting-edge technologies while contributing to meaningful advancements in clinical research. Join us in the UK and be part of a team that not only prioritises your career development but also fosters a sense of belonging and purpose.
