Clinical Data Monitor

<h2>Job Overview:</h2><p style="margin-bottom: .0001pt;"><span style="font-family: arial, helvetica, sans-serif; color: black; font-size: 10pt;">Your new employer is <span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Labcorp Drug Development</span>, the world’s most comprehensive drug development company, dedicated to improving health and improving lives. Our unique perspectives, built from decades of scientific expertise and precision delivery of the largest volume of drug development data in the world, along with our innovative technology solutions, help our clients identify new approaches and anticipate tomorrow’s challenges as they evolve. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career. </span></p><p style="margin-bottom: .0001pt;"><span style="font-family: arial, helvetica, sans-serif; color: black; font-size: 10pt;"> </span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;"><span style="color: black;">This is your chance to become part of a team that helps to bring the miracles of medicine to market sooner.</span> <span style="color: black;">Excellent opportunity for a <span style="font-size: 10pt; font-family: arial, helvetica, sans-serif; color: black;">Clinical Data Monitor </span>to join <span style="font-size: 10pt; font-family: arial, helvetica, sans-serif; color: black;">the Clinical Pharmacology Team within the European Centre of Excellence in the heart of Leeds, West Yorkshire on permanent basis. </span></span></span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif; color: black;"> </span></p><p style="margin-bottom: .0001pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"><strong><u>Key Responsibilities</u></strong></span></p><p style="margin-bottom: .0001pt;"> </p><p style="margin-bottom: .0001pt;"><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Your main responsibilities will include but not be restricted to: </span></p><ul><li style="color: #000000;"><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Data Planning – responsible for all data aspects of studies including review of draft protocols, attending Clinic Start Up Meetings, supporting the workbook (CRF) design process, training plans for non-standard study data capture and attend Biometrics start up meetings as required.</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Ensure that the data entry and QC of dose escalation data is completed within the required timelines.</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Complete daily ongoing QC of all study data across Clinical Operations including daily shop floor QC.</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Act as principle host for sponsor CRF monitoring visits. Promoting a professional image of Leeds CRU and building strong collaborative working relationships with CRA’s.</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Query Resolution – ensure all database queries; sponsors written data queries, CRA monitoring queries and internal QA audit findings are resolved within the agreed timelines. </span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Responsible for ensuring the weekly Data Entry Schedule is updated and accurately reflects study workload.</span><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"><em> </em></span></li></ul><h2>Education/Qualifications:</h2><ul><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Educated to GCSE / O level standard. Or in lieu of education relevant job experience will be considered.</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Must be able to demonstrate working knowledge of Microsoft Office.</span></li></ul><h2>Experience:</h2><ul><li><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">1-2 years of data handling experience. Experience can be from a clinical or non-clinical background. For example financial data handling background.</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Excellent written and oral communication skills.</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Ability to prioritize workloads.</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Good organizational skills.</span></li><li style="color: #000000; font-family: 'Times New Roman',serif; font-size: 11pt;"><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">Previous customer service experience desirable.</span></li></ul><p style="margin: 0px;"><span style="font-size: 10pt; font-family: arial, helvetica, sans-serif;">#LI-SP2</span></p>