Learning Management System (LMS) Administrator

Who we are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials , and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!
*SUMMARY:* *The Senior Learning Management System (LMS) Administrator is responsible for assisting Worldwide Clinical Trials Departments and LMS Support Team in all the aspects of LMS administration and maintenance as directed by the Associate Director of Learning Management Systems. The Senior LMS Administrator is responsible for creating course workflows and maintaining training assignments in Worldwide’s Learning Management System (LMS), providing ongoing support to the user base, and resolving LMS related requests and issues in a timely manner.**RESPONSIBILITIES:*_Tasks may include but are not limited to:_Proficient in the maintenance of the global Learning Management System (LMS) Create learning-related activities (e.g., training modules, classes, courses, learning matrices, etc.) within the LMS for SOPs, work instructions, Job Specific, and Study Related training.Resolves LMS related queries from the end user communityMaintains the LMS support center, including appropriate documentation, interacting with Worldwide Clinical Trial’s IT department, and the software vendor to resolve issues in a timely manner, minimizing system downtimeCreates and maintains system guidelines and FAQs to ensure consistent operation by end users Provide support with the retrieval of training records, plans and related documents during audits and inspection. Provide responses to audit and inspection training related findings. Manage user accounts in the LMSAssist with developing standards, processes, procedures, guidelines, and quality checks to maintain system configurations, architecture, and role-based security with consistency across activitiesResolve specific training problems and provides consultation on effective solutionsProvide training related reports to the business, using the LMS reporting functionalityTrain and mentor new team membersLead training department projects as assigned. Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.* OTHER SKILLS AND ABILITIES:*Strong working knowledge of learning management systems and their principles of operationStrong knowledge in all MS-Office applications including Microsoft Word, Excel, and PowerPoint.Excellent written and verbal communication skills, including negotiation skills and knowledge to clearly and concisely present information.Strong ability to plan, strategize, manage, monitor, schedule, critique, and problem-solveManaging, monitoring, scheduling support tasks according to service level agreements in the Worldwide support center.Exhibit basic project management skillsDemonstrate strong customer service skillsExhibit knowledge of the CRO/pharmaceutical industryAbility to create strong