Medical Writer – Clinical Evaluation Reports Pacific time zone only
Job Ref: JOB-45850
Our client is an In-Vitro Diagnsotic (IVD) developer/manufacturer. The company has had multiple ownership transitions over the previous several years. They are currently updating many files to be compliant with the upcoming IVDR requirements ((EU) 2017/746 of the European Parliament and of the Council of 5 April 2017).
They are seeking help from a medical writer or writers to create Clinical Evaluation Reports and possibly assist with Technical File creation. There are many files, but much of the material in each file is boiler plate since all the products are manufactured in essentially the same manner. Having a good understanding and knowledge of different types of cancers and antibodies would be desired.
The client would like to get started soon and anticipating the project to take 9 – 12 months. They are requesting candidates on the West coast so they are in the same time zone.