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Project Training Coordinator (Supporting Clinical Project Teams)

Laboratory Corporation of America Holdings (Covance)

Bangalore, India

<p><b>Responsibilities:</b></p><ul><li>Facilitate the creation, revision or inactivation of all project training requirements in the LMS</li><li>Provide regular updates to project leaders and project coordinators on the status of all project related training requirements </li><li>Monitoring and tracking compliance of study teams to training requirements leveraging LMS reporting capabilities and excel</li><li>Send notifications to team members that are delinquent in completing training requirements</li><li>Escalation of repeated delinquent training requirements to project leads</li><li>Assign & remove role based curricula to staff members throughout the life of the study</li><li>Ensure accuracy and quality of all assignments and curricula for which they are responsible</li><li>Administer updates to assignments and curricula in the LMS</li><li>Run ad hoc reports from the LMS as needed</li><li>Perform regular reconciliations between LMS generated compliance reports and project team maintained directories</li><li>Extract from the LMS and file training records of all team members in the Trial Master File at study close</li><li>Ensure all training requirements are removed and inactivated at study close out </li><li>Support Project Training Supervisors with ad hoc requests</li><li>Assist the Learning Operations & Solutions Strategy function as required with ad hoc tasks</li><li>Perform other administrative duties as assigned by management </li></ul><p></p><p><b>Education and Experience needed:</b></p><ul><li>Bachelor's degree -preferably in life sciences</li><li><b>Minimum two (2) years administrative experience in Clinical Operations department or 1 year of LMS (Saba Cloud) experience preferred   </b></li><li>Advanced knowledge of Excel and ability to analyze data</li><li>Experience with SharePoint </li><li>Management of multiple projects</li><li>Experience working on teams Understanding of clinical trials & GCP </li><li>Knowledge of LMS a plus</li><li>Data Entry Skills Quality & compliance tracking  </li><li>Aptitude for handling and reviewing numerical and written data</li><li>Excellent organizational and time management skills</li><li>Fluency in English, both written and verbal</li><li>Ability to work self-directed with minimal supervision</li><li>Organized with a meticulous eye for detail</li></ul><p></p><p><b>Labcorp is proud to be an Equal Opportunity Employer:</b></p><p></p><p>As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.</p><p></p><p>For <span>more information about how we collect and store your personal data, please see our </span><span><a href="https://www.labcorp.com/hipaa-privacy/web-privacy-policy" target="_blank">Privacy Statement</a></span><a href="https://www.labcorp.com/hipaa-privacy/web-privacy-policy" target="_blank"><span>.</span></a><span> </span></p>

Job posted: 2022-03-29

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