Study Coordinator Crop Protection-Study Coordinator Toxicology

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-family: 'times new roman', times; font-size: 12pt;">As part of an expansion of our Crop Protection & Chemicals (CP&C) capabilities in the US we have an</span><span style="font-family: 'times new roman', times; font-size: 12pt;"> exciting opportunity for <strong>Study Coordinator Crop Protection & Chemicals (CP&C)</strong> to join our team in Greenfield, IN.</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: 'times new roman', times; font-size: 12pt;">In this position you will work closely with Reserach Assistants, Study Directors and our clients by coordinating activies for chemical toxicology studies.. </span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: 'times new roman', times; font-size: 12pt;"><span style="font-family: 'times new roman', times;"><strong> Study Coordinator Crop Protection</strong> will apply their knowledge in Chemical Toxicology studies by 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. Common duties include but not limited to;</span></span></p><ul><li><span style="font-family: 'times new roman', times; font-size: 12pt;"><span style="font-family: 'times new roman', times;">Provides support for toxicology studies, including prestudy tasks (e.g., protocol development, costing, scheduling), monitoring the inlife progress of assigned studies, and interacting with clients including</span> prestudy tasks (e.g., protocol development, costing, scheduling), monitoring the in life progress of assigned studies, and interacting with clients.</span></li><li><span style="font-family: 'times new roman', times; font-size: 12pt;">Serves as administrative backup for Study Directors on day to day study-specific activities or tasks.</span></li><li><span style="font-family: 'times new roman', times; font-size: 12pt;">Coordinates the study award process as applicable, c</span><span style="font-family: 'times new roman', times; font-size: 12pt;">oordinates the efforts of a study team to become a successful project manager.</span></li><li><span style="font-family: 'times new roman', times; font-size: 12pt;">Will plans, prioritize, and manage a workload and the associated responsibilities.</span></li><li><span style="font-family: 'times new roman', times; font-size: 12pt;">Serves as a contact in communication and interactions with other departments and clients, with assistance as applicable.</span></li><li><span style="font-family: 'times new roman', times; font-size: 12pt;">Maintains complete, organized, and current study files including study schedule, protocol, and applicable correspondence.</span></li><li><span style="font-family: 'times new roman', times; font-size: 12pt;">Schedules and participates in preinitiation and other study-related meetings, as required, and takes and distributes preinitiation meeting minutes.</span></li><li><span style="font-family: 'times new roman', times; font-size: 12pt;">Drafts and submits appropriate documents to the IACUC/AWERB for approval</span></li><li><span style="font-family: 'times new roman', times; font-size: 12pt;">Verifies the project schedule accurately reflects the requirements of the protocol and monitors </span><span style="font-family: 'times new roman', times; font-size: 12pt;">progress and status of assigned studies.</span></li><li><span style="font-family: 'times new roman', times; font-size: 12pt;">Addresses and reviews quality assurance audits relating to protocols and amendments and reports (as applicable), with oversight. Follows up with appropriate personnel to ensure all necessary document/data clarifications are completed in the specified timeliness.</span></li></ul><p style="margin: 0px;"><strong><span style="font-family: 'times new roman', times; font-size: 12pt;">Why Labcorp Drug Development?  </span></strong></p><ul><li><span style="font-family: 'times new roman', times; font-size: 12pt;">See why FORTUNE magazine has named Labcorp as one of the <a href="https://fortune.com/company/laboratory-corp-of-america/worlds-most-admired-companies/" target="_blank" rel="noopener">Worlds Most Admired Companies</a> for 3 years in a row! </span></li><li><span style="font-family: 'times new roman', times; font-size: 12pt;">Full time position with outstanding benefits that begin the first of the month</span></li><li><span style="font-family: 'times new roman', times; font-size: 12pt;">24 days of PTO the first year with outstanding growth potential </span></li><li><span style="font-family: 'times new roman', times; font-size: 12pt;">You work will contribute to our mission to advance health and power clear and confident decisions. </span></li></ul><h2>Education/Qualifications:</h2><p style="margin: 0px;"><span style="font-size: 12pt; font-family: 'times new roman', times;">Bachelor’s degree in Biology or related science field (some related fields include but not limited to biochemistry, toxicology, animal science, and chemistry)  along with  </span><span style="font-size: 12pt; font-family: 'times new roman', times;">2 or more years of experience Chemical Toxicology studies preferred but not required.  </span></p><h2>Experience:</h2><p style="margin: 0px;"><span style="font-size: 12pt; font-family: 'times new roman', times;">Highly prefer candidates with 1 or more years of  experience performing research toxicology studies including small animal research studies.  Experience may be a substitute for education </span><span style="font-size: 12pt; font-family: 'times new roman', times;">Developmental and reproductive toxicology small animal research experience is preferred.</span></p>