♦ In this position candidates complete the Covance Monitoring Excellence Academy (MEA) training program ♦ Provide clinical support for projects according to Covance Standard Operating Procedures, ICH Guidelines and GCP ♦ Develop and/or maintain tracking systems for clinical projects ♦ Assist teams and conducts site monitoring of clinical research studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP ♦ Site management responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP
We are looking for a minimum of three to six months' monitoring experience. Ideally Perth based.
University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure)
Minimum of 2 years of experience in a related role (e.g. site management, in-house CRA, study coordinator, research nurse, etc.)
♦ Internal candidates o Internal candidates with a minimum 2 years clinical trials or site management experience (e.g. study coordinator, project coordinator, project specialist, study start up) ♦ Ability to monitor study sites according to protocol monitoring guidelines, SOPs, ICH Guidelines and GCP ♦ Ability to work within a project team ♦ Good planning, organization and problem solving abilities ♦ Good communication skills, oral and written ♦ Good computer skills ♦ Works efficiently and effectively in a matrix environment ♦ Fluent in local office language and in English, both written and verbal
Preferred: ♦ One (1) or more additional years of experience in a related field (i.e., medical, clinical, pharmaceutical laboratory, research, data analysis, data management or technical writing) is preferred.
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