Description
Are you a Regulatory Affairs Consultant based in Europe or the USA?
Are you looking for an exciting new opportunity working for a large biopharmaceutical company?
If this sounds like a good fit for you then apply below!
The role is for a consultant who will author CMC portion of Pre-IND-Meeting Request Letter and Briefing document. Also, author Modul 2.3 and Module 3, who also has working experience within Oncology – Solid Tumors.
