Senior Real-World Evidence Medical Writer

The role

Protocols, informed consent forms and study reports for late-phase safety and real-world evidence studies are the core output, along with abstracts, posters and manuscripts built from the statistical results. You also run quality control on the team's writing and join bid-defence presentations. Remote across the UK and a spread of European countries, with four or more years of medical writing in pharma, biotech or a CRO and an advanced science degree or PharmD.

Tools and skills