Vacancy

QA/GCP CO-ORDINATOR

Location: LONDON

Job Specification: The post is funded through the Cancer Research UK programme grant for 2 years. The post would suit an enthusiastic and self-motivated individual with considerable experience in clinical trials involving Investigational Medicinal Products, including significant experience in SOP writing. We are looking for someone with a degree, or equivalent, and an excellent understanding of relevant current national and European clinical trial regulations. Experience of audit and or GCP inspections, an ability to assimilate information from many sources and compile into workable documents and excellent writing skills are also essential.

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