Description
I have a Regulatory Medical Writer (Clinical Documents/Clinical Study Reports/Investigator Brochures) requirement for a global organisation. The position is a Contract to PERM position for a Regulatory Medical Writer to be based in RPT, North Carolina.-Extensive experience in Clinical Documents:
-Clinical Study Reports (CSR) -Investigator's Brochures (IB).
-The ability to understand and interpret data into drafts of CSR's
-Performed literature reviews
-Prepare clinical sections of IND submissions (module 2)
-BA/BS degree in life sciences Advanced degree preferred (MS, Phd or Pharma D)
If you are interested, please attach an up to date CV and I will be in touch.
To find out more about Real please visit www.realstaffing.com