Do you have 6-12 months monitoring expereince? Would you like to work in a dedicated role fully outsourcded in an exclusive role for one single sponsor? 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)
o A minimum of 2 years of experience in a related role (e.g. site management, in-house CRA, study coordinator, research nurse, etc.)
♦ Basic understanding of ICH Guidelines and GCP including a basic understanding of regulatory requirements ♦ Basic understanding of the clinical trial process ♦ Valid Driver’s License
Preferred: ♦ Working knowledge of Covance SOPs for site monitoring
Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
Share on your newsfeed