Study Coordinator - Toxicology

<h2>Job Overview:</h2><p style="margin: 0px; text-align: justify;"><strong><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Are you proactive, enjoy working with people and have a keen interest in toxicology?</span></strong></p><p style="margin: 0px; text-align: justify;"> </p><p style="margin: 0px; text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;"><strong>Are you looking to take the next step in your career?</strong></span></p><p style="margin: 0px; text-align: justify;"> </p><p style="margin: 0px; text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;"><strong><span style="color: #000000;">At our site in Huntingdon we are looking to recruit a Study Coordinator to join the team.</span></strong></span></p><p style="margin: 0px; text-align: justify;"> </p><p style="margin: 0px; text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;"><strong><span style="color: #000000;"><span style="font-size: 12pt; font-family: Arial, sans-serif; color: #000000;">Labcorp Drug Development is a global, world-leading Life Sciences Contract Research Organisation that provides dedicated and fully comprehensive laboratory testing and drug development services to the pharmaceutical, crop protection and chemical industries. We strive to make a difference to people’s everyday lives by bringing essential medicines to the market.</span></span></strong></span></p><p style="margin: 0px; text-align: justify;"> </p><p style="margin: 0px; text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">The <strong>Study Coordinator</strong> is responsible for coordinating the activities of routine and non-routine toxicology studies, in compliance with the appropriate company standards, Home Office requirements and regulatory guidelines, in a timely, efficient manner.</span></p><p style="margin: 0px; text-align: justify;"> </p><p style="margin: 0px; text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">This role offers flexible working with the opportunity for some remote working and is an excellent option for those that already have experience in a similar role or within the pre clinical toxicology arena looking for progression.</span></p><p style="margin: 0px; text-align: justify;"> </p><p style="margin: 0px; text-align: justify;"><strong><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"> The Study Coordinator:</span></strong></p><ul style="text-align: justify;"><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Provides scientific and administrative support to the Study Director for assigned toxicology studies from award, through the in-life phase. This involves multiple study set up tasks including protocol development, scheduling and initiation meetings</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Proactively liaises with clients, study monitors, Principal Investigators and internal departments to ensure accurate and timely protocol and amendment development and distribution</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Works with key clients and learns to implement action plans for solving study problems as they occur, including participation in client issue resolution process and any associated internal or external discussion</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Co-hosts or independently hosts client visits. May also assist with regulatory visits as appropriate</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Possesses the ability to mentor and train less experienced staff members</span></li></ul><p style="margin: 0px; text-align: justify;"> </p><p style="margin-bottom: 0.0001pt; text-align: justify;"><span style="color: #000000;"><strong><span style="font-size: 12pt; font-family: Arial, sans-serif;">We can offer you:</span></strong></span></p><ul><li style="text-align: justify;"><span style="font-size: 12pt; font-family: Arial, sans-serif; color: #000000;">Exposure to a variety of studies and the opportunity to interact with all departments involved in pre-clinical toxicology studies <span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">from client managers to reporting teams. This enables opportunities to develop knowledge, progress within the team and potentially to wider roles in Safety Assessment in the future.</span></span></li><li style="text-align: justify;"><span style="font-size: 12pt; font-family: Arial, sans-serif; color: #000000;">Competitive salaries and a comprehensive benefits package including health cover and contributory pension</span></li><li style="text-align: justify;"><span style="font-size: 12pt; font-family: Arial, sans-serif; color: #000000;">Unrivalled opportunities to develop a successful career in the scientific industry</span></li><li style="text-align: justify;"><span style="font-size: 12pt; font-family: Arial, sans-serif; color: #000000;">Unsurpassed career development opportunities where you can learn as you develop in a supported team environment</span></li><li style="text-align: justify;"><span style="font-size: 12pt; font-family: Arial, sans-serif; color: #000000;">Flexible working</span></li></ul><h2>Education/Qualifications:</h2><ul><li style="text-align: justify;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: #000000;">BSc, preferably Life Science degree. Experience may be substituted for education</span></li></ul><h2>Experience:</h2><ul><li style="text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;">Significant demonstrable experience in Toxicology or Study Coordination</span></li><li style="text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;">Demonstrates excellent communication and time management skills</span></li><li style="text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;">Excellent attention to detail and consistent accuracy whilst managing multiple changing priorities</span></li><li style="text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;">Knowledge of GLPs, regulatory agency guidelines and Home Office requirements</span></li></ul>