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Clin Res Assoc ICovance
Job Overview: Do you have 6-12 months monitoring experience? Would you like to gain broader experienced working on multiple studies for various sponsors? Look no further ♦ Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, with or without guidance liaise with vendors ♦ Responsible for aspects of registry management as prescribed in the project plans ♦ General On-Site Monitoring Responsibilities Minimum Required: - University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure) - Basic knowledge of Regulatory Guidelines - Basic understanding of the clinical trial process - Fluent in local office language and in English, both written and verbal Preferred: - Working knowledge of Covance SOPs regarding site monitoring Minimum Required: - Six (6) months experience in a related role (e.
g. site management, in-house CRA, study coordinator, research nurse, etc.) - Basic understanding of Regulatory Guidelines - Ability to work within a project team - Good planning, organization and problem solving skills - Good computer skills with good working knowledge of a range of computer packages - Works efficiently and effectively in a matrix environment - Valid Driver's License Preferred: - One (1) or more year's additional experience in a related field (i.
e. medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred - 6 months on site monitoring experience.