Study Coord V

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-family: 'Times New Roman',serif; font-size: 12pt;">The Study Coordinator is responsible for coordinating the activities of routine and non-routine studies, in compliance with the appropriate company standards, GLP and regulatory guidelines in a timely, efficient manner. General assistance to Study Directors will be an essential part of the role and additional non study specific support may be given to key clients. Additional daily duties may include support of other functions within Safety Assessment and will include training and mentoring of other Study Coordinators. This position also begins to apprentice under the mentorship and guidance of Study Directors to develop general expertise in toxicological assessment.</span></p><h2>Education/Qualifications:</h2><p style="margin: 0px;"><span style="font-family: 'Times New Roman',serif; font-size: 12pt;">Prefer Master's degree or Bachelor with a related experience.</span></p><h2>Experience:</h2><h2 style="margin: 0in 0in 0pt 0.25in;"><span style="font-family: times new roman,times; font-size: 12pt;"><span style="font-family: 'Times New Roman',serif;">Prefer 35 years’ knowledge or experience in Toxicology</span></span></h2>