<br /><p><span style="color:#16191f"><span>Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives.</span></span></p><br /><p><b>Ichem Study Coordinator</b></p><p>Labcorp is seeking an <b>Ichem Study Coordinator</b> to join our team in <b>Shanghai, China</b>. </p><p></p><p><b>Job Responsibilities:</b></p><ul><li>Independently drafts protocols, sample analysis outlines (SAOs), amendments and study schedules with some oversight, using proposal outline or client-supplied information.</li><li>Responsible for report preparation, including table and figure preparation. Compiles analytical information from laboratory groups.</li><li>Responsible for data table compilation including quality review oversight and data table transfer.</li><li>Communicates and interacts with study team, other departments and clients as applicable.</li><li>Serve as the primary contact in communication and interaction with other departments and clients as applicable.</li><li>Proven ability to plan, prioritize and manage workload and multiple responsibilities.</li><li>Demonstrated ability to independently use project tracking systems as appropriate.</li><li>Maintains well documented, organized and up-to-date study files including study schedule, protocol and correspondence as applicable.</li><li>Assists SD/PI in monitoring study progress.</li><li>Serves as a backup PI/SD on project management tasks</li><li>Schedules study phases in coordination with SD/PI and lab operations.</li><li>Proven ability to participate in and assist Study Director/Principal Investigators with pre-initiation and other study related meetings as required.</li><li>Proven ability to manage increasingly complex projects and study designs and/or increased study load.</li><li>Demonstrated capability to manage work for key clients.</li><li>Demonstrated ability to support and be involved in process improvement initiates and endeavors</li><li>Reviews QAU report audits. Submits audit responses for approval as appropriate. Follows up with appropriate personnel to ensure that all necessary report/raw data clarifications are completed within specified timelines.</li><li>Assists with routine client visits as requested.</li><li>Performs other related duties as assigned</li><li>Assists in setting up and performing method development and validation of various analytes in a variety of matrices.</li><li>Performs complex analyses using unfamiliar or new methods, asking for scientific guidance as needed.</li><li>Makes suggestions for modifications in test methods or procedures</li></ul><p></p><p><b>Minimum Required:</b></p><ul><li>Bachelor Degree in pharmacy, pharmaceutical analysis or chemistry. </li><li>3 months or more experience using computer and office software applications (e.g. Microsoft Word, Excel, MS-Access and Outlook). </li></ul><p></p><p><b>Preferred Qualifications:</b></p><ul><li>Two years of study coordinator for large molecule.</li><li>Efficient use of word processing software, database, spreadsheet, and specialized software.</li><li>Proficient in concise writing. Writing should require little or no external review or edit.</li><li>Adherence to grammar, punctuation, composition, and spelling according to company standard conventions.</li><li>Experience on a variety of studies performed in the department and exposure to a diverse client base.</li><li>Knowledge of regulatory agency guidelines.</li></ul><p></p><p><b>Additional Job Standards:</b></p><ul><li>Excellent communication, presentation, and interpersonal skills.</li><li>Excellent attention to detail.</li><li>Efficient in prioritizing and managing time.</li></ul><p></p><p>At Labcorp we have a passion for helping people live happy and healthy lives. Every day we provide vital information that helps our clients and patients understand their health. If you are passionate about helping people and have a drive for service, then Labcorp could be a great next career step! </p><p></p><br /><p><b>Labcorp is proud to be an Equal Opportunity Employer:</b></p><p>Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law. </p><br /><p><b>We encourage all to apply</b></p><p>If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our <a target="_blank" href="">accessibility site</a> or contact us at <a target="_blank" href="mailto:Disability_apply@LabCorp.com">Labcorp Accessibility.</a> For more information about how we collect and store your personal data, please see our <a target="_blank" href="">Privacy Statement</a>.</p><br />