Regional Study Coordinator

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. Regional Study Coordinator Labcorp is seeking a Regional Study Coordinator to join our team in Shanghai, Beijing, Guangzhou, Suzhou or Dalian, China.

Act as regional liaison between Global Study Manager and various LCLS departments involved in the study. Act as regional liaison between assigned Client representatives (eg. CRA, Site Monitors)and the corresponding local LCLS platform; occasionally, the Regional Study Coordinator can represent Global Study Manager in interactions with the main client contact. Close collaboration with the Global Study Manager for all study related aspects that are pertaining to the corresponding local platform and through all study stages, from set-up to closure. Review the study Statement of Work to ensure local feasibility and make appropriate recommendations to the Study Design Lead. Ensure a detailed knowledge of the SOW specifications and very good understanding of how the SOW specifications impact every operational aspect of the clinical trial. Manage day-to-day local study related activities, especially logistics, monitoring and study supplies, keeping the Global Study Manager informed of any study development. Monitor, track and provide resolution to all local study issues, keeping the Global Study Manager in the communication loop. Responsible for implementing monitoring and setting up of local performance metrics and taking corrective actions when needed. Liaise with the Global Study Manager for any tasks assigned to the Regional Study Coordinator as part of the Global Monitoring Plan. Demonstrate ability to work in a matrix environment where task assignments can be channeled down to be completed by Regional Study Coordinators while other task assignments will need to be delegated to other functional groups; demonstrate flexibility in handling both categories of tasks. Participate in functional meetings (eg. CLFs) and provide input, keeping processes up to date. Comply with LCLS Global Project Management strategy. Support a culture of continuous improvement, quality and productivity. The Regional Study Coordinator is expected to interact internally on a regular basis and occasionally with external clients throughout all job duties mentioned above. Other duties as assigned.

Bachelor Degree in Life Sciences or Pharmaceuticals. 3 months or more experience using computer and office software applications (e.g. Microsoft Word, Excel, MS-Access and Outlook).

2 or more years of customer service experience in pharmaceutical industry. Proficiency in English.    Additional Job Standards: Strong interpersonal skills. Influence and negotiation skills. Demonstrated ability to plan and prioritize. Demonstrated communication and organizational skills. Demonstrated attention to detail. Demonstrated participation in process improvement initiatives. Proven ability to excel in a fast-paced environment. Proven teamwork. Proven experience and knowledge of processes and tools used in department. Demonstrated ability to liaise with internal departments.