16/04/2024 | Fulltime | Didcot | CV-Library | £40,000 - £60,000 / Year Requirements and guidelines, including GCP and ICH. - Familiarity with clinical trial data management systems and electronic data capture. - Experience with site selection, initiation, management, and monitoring activities. Desirable Skills & Qualifications - Certification in clinical research, such as ACRP
Save for laterRegister your CV12/03/2024 | Fulltime | Abingdon | CV-Library | £240,000 - £280,000 / Year Requirements. At least 3 years of relevant experience in clinical drug development, including early phase trials. At least 2 years of experience as a medical monitor in biotechnology/pharmaceutical industry or CRO. Benefits This position is eligible for standard company benefits, including medical, dental
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