Medical Writer - CRO - 6 month contract
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
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