Regional Study Coordinator - 1 Year Contract

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. Labcorp is seeking a remote Regional Study Coordinator to join our team in Poland on a 1 year contract! work schedule: Monday - Friday Job Responsibilities: Manage the day-to-day activities of a clinical trial at a regional level. RSCs manage multiple studies and the responsibilities for each include: Collaborate with the Global Study Manager for all local study related aspects. Specifically, study set up and closure; ordering of study start up supplies, answering CRA questions regarding country specific regulations, etc. Act as regional liaison between Global Study Manager and various CLS departments involved in the study. Act as a regional liaison between assigned client representatives (e.g., Clinical Research Associates (CRAs) or Site Monitors) and LabcorpCLS internal departments and teams. Monitor, track and provide resolution to all local study issues; especially logistic issues and/or delays in receipt of study supplies, all the while keeping the Global Study Manager in the communication loop. Clean the laboratory database; e.g., a lab sample has been placed on hold and is not being analyzed, determine why it is not being processed and then resolve the issue. Deliver outstanding customer service and timely responsiveness to ensure client satisfaction, which requires a clear understanding of study design and major budget drivers. Work in a matrix environment where some task assignments are being channeled down to be dealt with by RSCs while other task assignments will need to be delegated by Regional Study Coordinators to other functional groups.

Bachelor degree 1 or more years of Clinical Project management experience within clinical studies Preferred Qualifications Master degree or University degree 1 or more years of experience in client communication Additional Job Standards Fluency in English 1 or more years of experience in Central Lab services Excellent communication and organization skills Demonstrated time management skills Dedicated to teamwork Ability to plan and prioritize Thrive in a fast-paced environment Get ready to redefine what’s possible and discover your extraordinary  potential. Here at Labcorp Drug Development, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you’ll be empowered to own your career journey with mentoring, training and personalized development planning.  Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow’s drug development challenges, creating new possibilities for our clients—and your career. The Company - LabCorp Drug Development As one of the world's largest and most comprehensive drug development services companies, LabCorp Drug Development has helped pharmaceutical and biotech companies develop one-third of the all prescription drugs in the marketplace today.

This position falls within our Central Labs Services group supporting