Clinical Research Associate I (19-00799) – AZ – Tucson


Clinical research coordinator with experience in a sponsor environment

In-house CRA experience preferred
Regional Monitor experience preferred
Experience in a Sponsor Environment
Experience in site visit preferred

*There is little monitoring experience available in this role, but there is some on site visit training potential and generally a less than 10% travel requirement. Could be more dependent on project needs

10% travel requirement.

*Would prefer at least 1-2 years prior research experience, in drug or device research.
*Previous experience with FDA/ICH/GCP
*Self motivating and a team player
*Proficient at managing multiple priorities and tasks
Source: Job Diva – Job Listing

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