Clinical Trials Administrator I

<h2>Job Overview:</h2><p style="margin: 0px;"><strong><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif; color: #1c1c1c; border: none windowtext 1.0pt; padding: 0in;">About Labcorp</span></strong></p><p style="margin: 0px;"><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif;">We are <span style="color: #444444;">Labcorp, a leading global life sciences company, named by Fortune magazine's 2021 List of World’s Most Admired Companies. </span>Thanks to the more than 70,000 amazing employees around the globe who make Labcorp a great place to work we continue to make the world a healthier and better place.</span></p><p style="margin: 0px;"><strong><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif; color: #1c1c1c; border: none windowtext 1.0pt; padding: 0in;"><br />The Opportunity</span></strong></p><p style="margin: 0px;"><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif;">The Clinical Project Team is responsible for the execution of a Clinical Research Project to evaluate a new medicine or treatment and to find out if new medical treatments or drugs are safe and effective.<br />As the Clinical Trial Administrator you will be an integral part of the team by ensuring the efficient functioning of the trial team by providing high-quality administrative support</span></p><p style="margin: 0px;"><strong><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif; color: #1c1c1c; border: none windowtext 1.0pt; padding: 0in;"><br />Key accountabilities will include (but not limited to)</span></strong></p><p style="margin: 0px;"><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif; color: #1c1c1c;"> </span></p><ul><li style="margin-left: .5in;"><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif;">Document and track study activities using relevant forms and tools, as well as relevant Project Management Systems </span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif;">Assist in the preparation of study and site specific materials in accordance with relevant (SOP’s) Standard Operating Procedures</span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif;">Complete minute taking and documentation for sponsor/external or internal teleconferences as requested </span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif;">Assist in setting up and maintaining tracking systems/spreadsheet for e.g. study supplies </span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif;">Provide support for Investigator Meetings; track meeting attendees and/or other information regarding the Investigator Meeting </span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif;">Provide support to project team (e.g. proof-reading and editing correspondence, mailings, shipping of study files, study documents, and arranging meetings, etc.) </span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif;">Set up and maintain clinical investigator files and documentation </span></li><li style="margin-left: .5in;"><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif;">Liaise with vendors, as needed, for study conduct such as printing study materials and/or external systems access for study team members. </span></li></ul><h2>Education/Qualifications:</h2><ul><li><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif;">Computer literacy (Microsoft Office Suite (Word, Excel, PowerPoint)</span></li><li><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif;">Aptitude for handling and proof-reading numerical data</span></li><li><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif;">Good spelling and proof-reading skills</span></li><li><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif;">Work efficiently and effectively in a matrix environment</span></li></ul><h2>Experience:</h2><ul><li><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif;">Minimum 1 year administrative experience (Preferably within the clinical or pharmaceutical industry)</span></li><li><span style="font-size: 10.0pt; font-family: 'Calibri',sans-serif;">Good organizational and time management skills</span></li></ul>