Clinical Research Coordinator

Clinical Research CoordinatorFlourish Research is where clinical trials thrive. Flourish Research is one of the industry's most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.About the Job:We are actively hiring a Clinical Research Coordinator to support our Chicago, IL site. Shift: Monday-Friday normal work hours Location: Onsite FLSA Classification: Non-Exempt Compensation: 65,000.00-$75,000.00Essential Job Functions:Read, understand, and can accomplish protocol specified patient visits and procedures.Clearly and concisely document patient assessments, observations, test results and other study related information per federal regulations, protocol requirements and GCPs.Obtain patient informed consent according to federal regulations, GCPs and IRB requirements.Is creative and diligent in recruiting qualified study subjects into assigned protocols to fulfill enrollment obligations within the sponsor's timeline while following regulations and rules governing medical ethics, IRB, GCP and ICH guidelines.Complete all required training in a timely manner.Schedule and conduct patient visits according to protocol requirements and timelines.Maintain accurate and complete written source documentation of patient visits and protocol related activities.Accurately complete case report forms (CRFs &/or eCRFs) and/or worksheets generated by the sponsor.Maintain confidentiality of patient and protocol issues as appropriate and as bound by Confidentiality Agreements with Flourish Research, between Flourish and sponsors, and between Flourish and other entities, as well as HIPAA regulations.Promptly report adverse events to supervisor and/or Principal Investigator/Sub-Investigator as deemed necessary.Report Serious Adverse Events (SAEs) to sponsor within 24 hours of becoming aware of the SAE.Also report the SAE to the supervisor, Principal Investigator and/or Sub-Investigator.Account for clinical trial materials (i.e., CRFs, study drug, lab supplies, and/or other required items) and ensure availability of appropriate amounts for the conduct of the study.Maintain ongoing communication with Team Lead I; Team Manager; Principal Investigator; Sub Investigators and other people assisting with the trial and documenting these communications according to protocol requirements and Flourish policies.Attend required training courses/conferences in order to stay abreast of current and changing federal regulations and Flourish policies.Pursue educational opportunities to increase knowledge of the research process and associated rules and regulations governing clinical research.Attend Investigator Meetings and/or other training as directed.Perform all study-related duties in a time- and cost-effective manner in adherence with Flourish policies.Perform all duties in a safe and prudent manner.Perform other duties as assigned.Represent Flourish Research in a professional and courteous manner (verbal, written and in appearance) when interacting with Flourish staff, sponsors, IRBs, patients/subjects, nursing and medical staff members of various clinics, hospitals, and physician's offices.Additional duties as assigned by management.Physical Requirements and/or Environmental Factors:Work is normally performed in a typical interior/office work environment.Travel required.Exposure to human bodily fluids.Laboratory processing procedures.Subject/Patient care.Daily computer use.Occasional night and weekend work schedules.The ability to properly lift thirty-five pounds and occasionally more than thirty-five pounds.The ability to drive, and daily availability of an automobile