The Clinical Research Coordinator 2 serves as a mid-level clinical research professional that assists in the planning, coordinating, implementing, monitoring, and evaluating of specific clinical research studies. This role assists in the day-to-day operations of clinical research protocol implementation and carries out study coordination duties from protocol initiation to study close-out according to regulatory/sponsor guidelines. The incumbent works closely with study team members and other staff/faculty/study sites to ensure study participant safety and adherence to approved protocols, help with study-related administrative tasks, facilitate across-the-board flow of information, and coordinate study activities and personnel. Core job functions include assisting in participant recruitment and retention, performing study procedures and data collection, specimen handling, maintaining study documentation, distributing study drug materials, monitoring adverse events, assisting with protocol amendments, study orientation, monitoring study progress, and administrative tasks related to study personnel. The role requires adherence to cultural competency guidelines and regulatory requirements, maintaining requisite skills and training, and safeguarding University assets. The position involves coordinating a large, multi-site R01/R37 study funded by the National Cancer Institute focused on metastatic cancer patients receiving immune checkpoint inhibitors. Responsibilities include recruiting, data collection and analysis, protocol interpretation, SOP development, study management, meeting coordination, REDCap data management, on-site visits and data collection, qualitative data analysis, literature reviews, recruitment efforts, report preparation, collaboration for publication, clinical data extraction from EHR/EMR, and continuing education. Occasional travel to San Antonio, Texas for site visits is required. The University of Miami offers competitive salaries and comprehensive benefits. The University is an Equal Opportunity Employer encouraging diverse applicants.
By applying, you consent to your information being transmitted by Jooble to the Employer, as data controller, through the Employer’s data processor SonicJobs.
See Sonicjobs Privacy Policy at and Terms & Conditions at and SonicJobs Privacy Policy at and Terms of Use at
Position Summary Manufacturing associate I is a hands-on position responsible for executing buffers and media for the upstream and downstream manufacturing process. The candidate will be responsible in the preparation of buffers related to all the manufacturing scale...
...ManTech seeks a motivated, career and customer-oriented Software Assurance Evaluation Engineer to join our team in Hanover, MD. This is a full time position with 5 days being onsite. The position is part of a team that provides software development support for an organization...
...convention centers, music festivals, performing arts centers, and cultural institutions on the planet . Position Summary: The Director of Food & Beverage is responsible for the efficient, professional and profitable operation of the food service operations at the...
...Koloma is a geologic hydrogen company that leverages its technology, proprietary data, and human capital advantages to identify and commercialize these resources on a global scale. We are developing technologies that will enable the production of low cost, reliable,...
...clinical support teams, and possible career growth opportunities. POSITION SUMMARY: The Service Coordination Supervisor - Early Intervention oversees all aspects of service provision for children receiving service coordination in the Early Intervention Program,...