Study Director I

<h2>Job Overview:</h2><ul><li style="margin-left: .25in;"><span style="font-size: 11.0pt;">Serve as a Study Director, as described in the GLPs. Has overall responsibility for the technical conduct of a study as well as for the interpretation, analysis, documentation, and reporting of results. </span></li><li style="margin-left: .25in;"><span style="font-size: 11.0pt;">Coordinates efforts of the study team.</span></li><li style="margin-left: .25in;"><span style="font-size: 11.0pt;">Develops develop protocols and ensures that the protocol, including any changes, is approved and is in compliance with appropriate SOPs, GLPs, and regulatory agency guidelines.</span></li><li style="margin-left: .25in;"><span style="font-size: 11.0pt;">Reviews cost estimates to ensure that all protocol/amendment driven workscope specifications have been included in the price estimation.</span></li><li style="margin-left: .25in;"><span style="font-size: 11.0pt;">Understands financial status of ongoing studies.</span></li><li style="margin-left: .25in;"><span style="font-size: 11.0pt;">Monitors progress and status of assigned studies. Ensures that all experimental data, including observations of unanticipated responses to the test system, are accurately recorded and verified.</span></li><li style="margin-left: .25in;"><span style="font-size: 11.0pt;">Directs analysis of data, preparation of reports, ensures compliance with protocol and regulatory requirements, and submits them to the client. </span></li><li style="margin-left: .25in;"><span style="font-size: 11.0pt;">Reviews the tabulated summaries as requested.</span></li><li style="margin-left: .25in;"><span style="font-size: 11.0pt;">Participates or hosts client visits </span></li></ul><p style="margin: 0px;"><span style="font-size: 11.0pt; font-family: 'Times New Roman',serif;">Performs other related duties as assigned.</span></p><h2>Education/Qualifications:</h2><p style="margin: 0px;"><span style="font-size: 11.0pt; font-family: 'Times New Roman',serif;">PhD or Master in toxicology or related subject, DVM or equivalent degree.  Experience may be substituted for education.</span></p><h2>Experience:</h2><p style="margin: 0px;"><span style="font-size: 11.0pt;">Zero to two years of related experience for PhD, and one to three year of related experience for Master.</span></p><p style="margin: 0px;"><span style="font-size: 11.0pt; font-family: 'Times New Roman',serif;">Skilled in performing scientific presentations and preparing scientific publications.</span></p>