Clin Res Assoc I

Job Number


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
• 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
• 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


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