Regional Study Coordinator – Central Labs Services, Clinical Research

Job Description: • Act as regional liaison between Global Study Manager and various CCLS departments involved in the study • Act as regional liaison between assigned Client representatives (eg. CRA, Site Monitors) and the corresponding local CCLS 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 Requirements: • Bachelor's degree preferred; High School Diploma required • At least two years of applicable experience • Demonstrated ability to plan and prioritize tasks and workload in a fast-paced environment • Exceptional communication and organizational skills • Excellent attention to detail and teamwork orientation • Demonstrated ability to facilitate meetings and work with clients Benefits: • Medical • Dental • Vision • Life • STD/LTD • 401(k) • Paid Time Off (PTO) or Flexible Time Off (FTO) • Tuition Reimbursement • Employee Stock Purchase Plan Apply tot his job