CRA II - Senior CRA - UK Wide

<h2>Job Overview:</h2><p style="margin: 0cm 0cm 0.0001pt; text-align: justify;"><span style="font-family: Arial, sans-serif; color: black; font-size: 12pt;">Exciti<span style="font-family: arial, helvetica, sans-serif;"><span style="font-size: 12pt;">ng news for <span style="color: black;">Labcorp Drug Development</span>, </span>new Sp</span>onsor coming!</span></p><p style="margin: 0cm 0cm 0.0001pt; text-align: justify;"><span style="font-family: Arial, sans-serif; color: black; font-size: 12pt;"> </span></p><p style="margin: 0cm 0cm 0.0001pt; text-align: justify;"><span style="font-family: Arial, sans-serif; color: black; font-size: 12pt;">Across the globe, we keep our commitment to improve health and improve lives, and at Labcorp we are looking for exceptional people who are eager to play an important role pushing new frontiers in how we diagnose, monitor and treat patients. </span></p><p style="margin: 0cm 0cm 0.0001pt; text-align: justify;"><span style="font-family: Arial, sans-serif; color: black; font-size: 12pt;"> </span></p><p style="margin: 0cm 0cm 0.0001pt; text-align: justify;"><span style="font-family: Arial, sans-serif; color: black; font-size: 12pt;">Our Drug Development business continues to support and meet the needs of our pharmaceutical and biotechnology client partners: we continue to initiate new studies from Early Development through Phase IV, and our Central Labs are fully operational. </span></p><p style="margin: 0cm 0cm 0.0001pt; text-align: justify;"><span style="font-family: Arial, sans-serif; color: black; font-size: 12pt;"> </span></p><p style="margin: 0cm 1.7pt 0.0001pt 0cm; text-align: justify;"><span style="font-family: Arial, sans-serif; color: black; font-size: 12pt;">In this spirit, we would like to keep growing our relationship with talented CRAs across the UK.</span></p><h2>Education/Qualifications:</h2><ul><li style="color: black;"><span style="color: black; font-family: arial, helvetica, sans-serif; font-size: 12pt;">Participates in initial and on-going protocol and CRF training at study site</span></li><li style="color: black; font-family: 'Times New Roman','serif'; font-size: 12pt;"><span style="color: black; font-family: arial, helvetica, sans-serif; font-size: 12pt;">May serve as the Primary contact for the clinical sites/Sponsor</span></li><li style="color: black; font-family: 'Times New Roman','serif'; font-size: 12pt;"><span style="color: black; font-family: arial, helvetica, sans-serif; font-size: 12pt;">Participates in the generation of study specific monitoring plans </span></li><li style="color: black; font-family: 'Times New Roman','serif'; font-size: 12pt;"><span style="color: black; font-family: arial, helvetica, sans-serif; font-size: 12pt;">May participate in identification and recruitment of investigators, collection of investigator documents and Pre-Study Visits </span></li><li style="color: black; font-family: 'Times New Roman','serif'; font-size: 12pt;"><span style="color: black; font-family: arial, helvetica, sans-serif; font-size: 12pt;">Participates in Sponsor and Investigator/Initiation Meetings</span></li><li style="color: black; font-family: 'Times New Roman','serif'; font-size: 12pt;"><span style="color: black; font-family: arial, helvetica, sans-serif; font-size: 12pt;">Tracks progress of assigned studies/projects and identifies appropriate actions to achieve target objectives.</span></li><li style="color: black; font-family: 'Times New Roman','serif'; font-size: 12pt;"><span style="color: black; font-family: arial, helvetica, sans-serif; font-size: 12pt;">Fulfils general on-site Monitoring Responsibilities</span></li><li style="color: black; font-family: 'Times New Roman','serif'; font-size: 12pt;"><span style="color: black; font-family: arial, helvetica, sans-serif; font-size: 12pt;">Prepares accurate and timely trip reports.</span></li><li style="color: black; font-family: 'Times New Roman','serif'; font-size: 12pt;"><span style="color: black; font-family: arial, helvetica, sans-serif; font-size: 12pt;">Identifies and completes follow- up of SAEs at study site for which he/she is responsible</span></li><li style="color: black; font-family: 'Times New Roman','serif'; font-size: 12pt;"><span style="color: black; font-family: arial, helvetica, sans-serif; font-size: 12pt;">Independently performs CRF review; query generation and resolution against established data review guidelines on Covance or client data management systems.</span></li><li style="color: black; font-family: 'Times New Roman','serif'; font-size: 12pt;"><span style="color: black; font-family: arial, helvetica, sans-serif; font-size: 12pt;">Assists with training of new employees, e.g. co-monitoring</span></li></ul><h2>Experience:</h2><ul><li style="color: black;"><span style="color: black; font-family: arial, helvetica, sans-serif; font-size: 12pt;">2 years of experience in a related field, including 2-4 years of independent on-site monitoring in CRO or Pharma</span></li><li style="color: black; font-family: 'Times New Roman','serif'; font-size: 12pt;"><span style="color: black; font-family: arial, helvetica, sans-serif; font-size: 12pt;">Experience in all Phase projects and PoC Studies</span></li></ul>