Our client company is a mid-sized CRO with global laboratory facilities. Due to growing business, and succession planning, the company has asked us to identify experienced Study Directors who might consider a career change.
A relevant graduate degree in Toxicology, or an adjacent science, and not less than two years of experience is required. Previous experience in a CRO setting is strongly preferred. A more experienced person (10+ years) would be considered for a site leadership role. The positions report to the company’s SVP of Toxicology/Safety Assessment.
Principal duties include the design, management and execution of GLP, in-vivo studies, report generation, client engagement, and contributing to proposals and business development activities. A more senior person would have a management role, in addition to the above noted activities.
The facility’s legacy is as a family based, high energy, collaborative work environment with bright and committed scientists. Relocation to the facility (in a large. Midwest metropolitan area) is required.
Search assignment #1539