Clinical Research Coordinator

About Us Flourish 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 race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation or veteran status. We embrace employees, customers, and patients from underrepresented groups to 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, ideas we share, and the better prepared we are to serve our communities. About the Job A Clinical Research Coordinator is needed to support our Chicago, IL site. Shift: Monday‑Friday, normal work hours Location: Onsite FLSA Classification: Non‑Exempt Compensation: $65,000.00 – $75,000.00

ESSENTIAL JOB FUNCTIONS

Read, understand, and perform protocol‑specified patient visits and procedures. 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. Recruit 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 & 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 and 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. Account for clinical trial materials (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 document these communications per protocol requirements and Flourish policies. Attend required training courses and conferences 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 appearance) when interacting with staff, sponsors, IRBs, patients/subjects, nursing and medical staff members of various clinics, hospitals, and physician's offices.

PHYSICAL REQUIREMENTS AND/OR ENVIRONMENTAL FACTORS

Work is normally performed in a typical interior/office 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 lift thirty‑five pounds and occasionally more than thirty‑five pounds. The ability to drive and have daily availability of an automobile. Requirements Bachelor's degree preferred; however, is not required. Preferably a minimum of 2 years of experience as a CRC, plus 1–3+ years' experience within the field of clinical research or biological research. Knowledge and Skills Exceptional knowledge of clinical research methods. Strong management and leadership skills. Demonstrated ability to collaborate and align with operations. Excellent oral and written communication skills. Excellent computer skills to include Office365 products. Experience in writing and reviewing standard operating procedures. Strong problem‑solving, risk assessment and impact analysis abilities. Demonstrated experience in process improvement. Strong negotiation and conflict management skills. Flexible and able to multi‑task and prioritize competing demands. Ability to think independently and influence when appropriate. Benefits Health, dental, and vision insurance plans; 401(k) with a 100% employer match on the first 4% of employee contributions; tuition reimbursement; parental leave; employee referral program; employee assistance program; life insurance; disability insurance; and a generous PTO plan covering vacation, sick, personal days and eight paid holidays. Flourish Research is an equal employment opportunity employer. Employment decisions are based on merit and business needs, and not on race, color, sex (including pregnancy and gender identity), citizenship status, national origin, ancestry, gender, sexual orientation, age, religion, creed, physical or mental disability, genetic information, marital status, veteran status, political affiliation, or any other factor protected by law. Flourish Research complies with the law regarding reasonable accommodation for handicapped and disabled employees. #J-18808-Ljbffr Flourish Research