I am working with a rapidly expanding Biotech, located in Belgium.
They are currently specializing in a range of exciting therapy areas and have the vision to be further innovators in the future.
With this they are looking to expand their team with two Quality Control Editors, being responsible for overseeing the content of clinical and regulatory documents from the medical writing team.
This position can be carried out as a freelancer role (home-based) and on a permanent basis anywhere in Europe, but able to travel to Belgium.
The main responsibilities are as follows:
- Performing quality reviews and editing clinical documents, regulatory documents, medical/ scientific documents
- Performs detailed QC review checks of clinical and regulatory documents, tables, publications, annual reports, literature summaries, submission sections, and internal documents.
- Proofreading and editing of documents
- Verify that documents are consistent with internal, client, and related authority guidelines.
- American English desired
- Sharepoint desirable
If you are interested in this exicitng role, please do apply to the Link and we will be in touch shortly.
