Description
I have a great opportunity for a Senior Regulatory Medical Writer (Reg/CSR/Protocols/Submissions). The Medical Writer will be required to have a proven track record in writing Protocols/ Protocol amendments CSR's, IB's and submission documents. The Regulatory Writer will be part of the client's oncology department and the contract is for 12 months extendable for a number of years.Regulatory Document experience required:
-Clinical Study Reports (CSR)
-Protocols and Protocol Ammendments
-Investigatory Brochures (IB's)
-Submission Documents
-Narratives
I am looking for someone with previous regulatory medical writing experience within a major pharma, ideally within Oncology however other therapeutic areas would be suitable. Please note, I am looking for someone from a regulatory background not with just Medical Education, Journal and Academia Experience ONLY.
If you are interested, please forward on an up to date resume and I will give you a call.
To find out more about Real please visit www.realstaffing.com