Associate Study Coordinator- PK/TK (Remote Possible)

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Labcorp Drug Development is currently seeking an Associate Study Coordinator for the Pharmacokinetic/Toxicokinetic (PK/TK) team at the Madison, WI site. <span style="color: black;">Remote working arrangement is a possibility.</span></span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">This position offers the opportunity to learn pharmacokinetics and toxicokinetics while also gaining client facing exposure. We are seeking motivated, career minded individuals who are interested in building a career with Labcorp Drug Development and the PK/TK team. The Study Coordination team offers a detailed and structured career pathway that provides the opportunity for rapid and accelerated advancement for determined individuals. Benefits include medical, dental, 401k, 24 days paid time off (plus additional holidays), community involvement opportunities, internal training and tuition reimbursement!</span></p><p style="margin: 0px;"> </p><p style="margin-bottom: 6.75pt;"><strong><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;"><span style="color: #000000;">We are offering a sign-on bonus of $3,000 ($1,500 upon hire and $1,500 after 6 months; external candidates only).</span></span></strong></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">As an Associate Study Coordinator your job duties will include:</span></p><ul><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Performs initial review of analytical data and originates noncompartmental analysis in support of pharmacokinetic and toxicokinetic studies</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Aids in report preparation, including tables and figures. Compiles analytical information from laboratory groups.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Assists in interpreting and evaluating data for reports</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Participates in and assists SD/PI with pre-initiation and other study related meetings as required</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Reviews progress and study status against initial work plan – maintains CMS with accurate schedules.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Proactively communicates and interacts with study team to ensure key milestones are achieved</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Serves as the primary contact in communication and interaction with other departments and clients as applicable</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Maintains well documented, organised and up-to-date study files including study schedule, protocol and correspondence.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Assists SD/PI in the PK/TK study phase, if applicable and review of study compliance with protocol, SOPs and regulatory guidelines.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Assists in the development and maintenance of standard report/table formats as required</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Participates in the editing process for scientific reports</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Reviews QAU report audits with SD/PI or appropriate laboratory group. Submits audit responses for SD/PI approval. Ensures that all necessary report/raw data clarifications are completed.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Learns to deputise for SD in their absence with ability to provide updates to internal/external customers</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Reviews client comments and makes decisions in conjunction with SD/PI and ensures that all necessary report/raw data clarifications are completed.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Regularly manages increasingly more complex projects and study designs and/or increased study load</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Responsible for and drives report production through finalization, including archiving of data as appropriate.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Prepares for and participates in routine client visits under direction of the SD/PI.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Maintains an awareness of the financial status of ongoing studies, including workscope changes</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Develops an area of expertise within the department and serves as a resource by providing training and written instructions</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Develops knowledge of Labcorp Drug Development metabolism capabilities such that they can coordinate (with supervision) one other area outside of their area of expertise</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Learns to expand responsibilities as a project coordinator for assigned clients(s) across the metabolism discipline</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Trains and mentors less experienced staff</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Able to review work of others for overall accuracy, timeliness, completeness and soundness of technical judgment.</span></li></ul><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-size: 8pt; font-family: Arial, sans-serif; color: #000000;">#LI-DZ1</span></span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="font-size: 8pt; font-family: Arial, sans-serif; color: #000000;"><span style="font-size: 8pt;"><span style="font-size: 11.0pt; font-family: 'Calibri',sans-serif;">#LI-REMOTE</span></span></span></span></p><h2>Education/Qualifications:</h2><ul><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Relevant degree plus 4 years' of appropriate experience. Relevant experience may be substituted for academic qualifications.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">At least 18 months at previous level.</span></li></ul><h2>Experience:</h2><ul><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Experience with Phoenix® WinNonlin® highly preferred.</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Ability to utilise word processing, databases, spreadsheets, and specialised software on personal computers.</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Skilled in the use of all standard laboratory equipment.</span></li></ul>