Job Description

This is an opportunity to be part of the growth and development of a highly successful CRO as it expends into the UK market place. The successful candidate will assist the Project Manger and/or monitor with the administration of clinical research projects.

The key functions of the role include:

Provide communication to Clinical Research Associates (CRAs), Principal Investigators, clinical suppliers, clinical laboratories, Project Manager and team members.
Provide functional guidance and keep Project Manager and lead CRA fully appraised of site and study status
Draft and prepare correspondence for mass distribution.
Draft regulatory documents for distribution to study sites and/or provide guidance regarding regulatory documents to CRAs in different countries.
Perform initial review and ensure completion of regulatory documents
Ensure regulatory documents are present throughout the duration of a study, and work with CRA to ensure they are current..

Qualifications/Skills Required

This opportunity will suit an individual with a B.A. / B.S. in the science/healthcare field or equivalent; at least 18 months experience in clinical research; experience in a CRO, or Pharmaceutical role; excellent English (both written and verbal) and computer knowledge (Word, Excel, Powerpoint, Email, Internet).