Are you an experience medical writer? Have a deep understanding of clinical development? Looking to work within a communicative, supportive work environment?
THEN I HAVE THE OPPORTUNITY FOR YOU!
After a recent partnership with a European leader in the production of radio pharmaceuticals, I am looking for motivated professionals to join the company in a Regulatory Medical Writer position.
The company develop, produce and commercialize molecular nuclear medicines, diagnostic and therapeutic products in the fields of neurology, oncology, cardiology and infectious diseases, as well as having a large pipeline across various phases.
As a Regulatory Medical Writer you will be responsible for writing clinical overviews & summaries, PIPs, scientific advice and responses, and clinical dossiers.
- Experience writing clinical dossiers (2.4,2.5,2.6,2.7)
- Strong understanding of clinical development
- Experience with scientific advice/responses, PIP’s, clinical overview and summary
For more information, APPLY NOW!