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FORTREA INC. Operations Coordinator I in MADISON, Wisconsin

JOB REQUIREMENTS: As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe. Operations Coordinator I Full-Time, on site in Madison, WI Responsible for practical/administrative activities in support of a clinical research trial. The Operations Coordinator I supports and assists the senior study team members such as the Clinical Research Coordinator and Project Manager as appropriate. Responsibilities: Responsible for logistical set up of study to ensure good study flow and adequate resources are assigned. Assists the Clinical Research Coordinator with their responsibilities and acts as their back-up as needed. Assists and/or is responsible for the creation of source documents, labels, and study specific instructions. Assists and/or is responsible for creation of study schedules. Orders supplies/equipment and dietary needs for assigned studies. Liaises with CRU contracted services, such as clinical labs and ECG services. Assists and/or is responsible for staff training of study specific procedures. Coordinates tasks related to participant check in and discharge and may assist with resolution of participant issues. Is present in the clinical work areas for critical events or as assigned by a senior team member. Completes sample shipment documentation as necessary. May assist with sample shipments as needed. Compiles data tables/summaries as requested. Assists with on-time CRF completion and query process as appropriate. Assists with the compilation of protocol and SOP deviations. Provide logistical feasibility for protocol development. Attends all required meetings as appropriate. Maintains skills to perform study tasks and assists with study procedures as necessary. Maintains accurate records of all work undertaken. Maintains an understanding of FDA, GCP and ICH requirements. Maintains... For full info follow application link. As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply. ***** APPLICATION INSTRUCTIONS: Apply Online: ipc.us/t/F751DBFAB494469B

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