As Regulatory Documentation Scientist you will prepare documents for submission to regulatory authorities. You will take accountability for writing and delivering regulatory documents, as well as interpreting scientific data and working closely with key content owners to establish key strategic messages. You will apply scientific writing, editing, document and project management expertise. Furthermore, you will contribute to the functional excellence of regulatory documentation through process management and strategic partnering.
To be considered for this fantastic opportunity you should have previous experience writing clinical or/and safety documents such as:
- Investigator Brochures (IB)
- Clinical Study Reports (CSR)
- Module 2 documents
Please ensure that this information is documented in your CV.
Keywords: Medical Writing, Medical Writer, Scientific Writer, Science Writer, Regulatory Affairs, Regulatory Writer, Regulatory, Pharma, Pharmaceutical, Contract, Temp, Home-based, Remote.
You must be eligible to work in the UK. Learn more
- Agency: Paramount Recruitment
- Reference: JG/MWR
Website: Paramount Recruitment
- Posted: 1st July 2021
- Expires: 29th July 2021