Our Client is a leading global CRO company based in South-East England. They require a Regulatory Medical Writer on an initial six month contract. You will be responsible for the medical writing for Phase II-IV clinical trials. Successful candidates will have the below experience • Writing regulatory and clinical documentation • Investigator Brochures • Clinical Protocols • Clinical Study Reports • Clinical Overviews • Knowledge of ICH and FDA • Organised You will need to have a higher degree in sciences or a health-related field (Master's Degree, PhD or equivalent) to be considered for the position. Experience in writing clinical study reports and manuscripts for publication is desirable. Candidates should have a commitment to quality, be flexible, organised, have good team skills and the ability to work to tight deadlines. KEYWORDS: MEDICAL WRITING, FDA, ICH, ICH-GCP, PHASE II-PHASE IV, CRO, PHARMA, REGULATORY, SENIOR, WRITER