Clinical Research Coordinator
$65k - $75kFlourishresearch
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 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. WESEEYOU. 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: 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 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 Qualifications: Bachelor's degree preferred; however, is not required. Preferably a minimum of 2 years’ experience as a CRC, plus 1-3+ years' minimum 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. 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 8 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 Flourishresearch
$36.06 - $40.87 per hour
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$51.35k - $64.47k
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...Description Clinical Research Coordinator - Clinical Trials IMA Clinical Research Chicago, IL Full-Time Permanent $60,000-$65,000, depending on experience At IMA Clinical Research, every study brings new therapies closer to the patients who need them. As a...Permanent employmentFull timeLocal areaFlexible hoursWeekend work- Position Title Clinical Research Coordinator I Department Global Project Delivery Job Type This role is a per-diem contract opportunity* About the Company Ora is a leading full-service ophthalmic drug and device development firm that guides clients across all phases...Daily paidFull timeContract workFlexible hoursWeekend work
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$27 per hour
The Clinical Research Coordinator II is responsible for the overall management and implementation of an assigned set of multiple research protocols ensuring efficiency and regulatory compliance. These studies will be conducted at the Loyola University Medical Center and...Hourly payWork experience placementLocal area- Rush University Medical Center in Chicago is seeking a Clinical Research Coordinator to work in the Pediatrics department. This full-time position involves recruiting and managing study participants, ensuring compliance with Good Clinical Practices and NIH/FDA regulations...Full time
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**Job Title:** Clinical Research Coordinator **Company:** HealthCare Enhanced **Location:** Chicago, IL **Salary Range:** $120,000 - $160,000 **Experience Level:** Experienced --- ### About Us HealthCare Enhanced is dedicated to advancing clinical research through...Full time$60k - $75k
...Department BSD NEU - Clinical Research Staff About the Department The Department of Neurology at The University of Chicago Medical... ...disease. Job Summary The Clinical Research Coordinator II (CRC II) is an onsite, patient-facing, specialized researcher...Work experience placement- A clinical research organization in Chicago is seeking a Clinical Research Coordinator I to ensure quality research is conducted at assigned sites according to protocols and regulations. The role involves conducting subject visits, documenting procedures, completing data...
$49.92k - $81.62k
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...Visiting Clinical Research Coordinator - Medicine, Chicago Breathe Center Job Posting extended until August 28, 2026 Hiring Department :Department of Medicine Location : Chicago, IL Requisition ID : 1071390 Posting Close Date : June 19, 2026 Salary:...Full timeWork at officeWorldwide$29.36 - $42.61 per hour
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About the Department The Office of Clinical Research (OCR) was created to further the research missions of the University of Chicago Biological... ...Research Operations Job Summary The Clinical Research Coordinator I (CRC I) supports routine assignments related to the documentation...Work experience placementWork at office$50k - $65k
The University of Chicago is looking for a Clinical Research Coordinator I to support clinical trials and ensure compliance with regulations. This role involves participant screening, enrollment, data management, and documentation across research studies. Applicants should...$50k - $65k
The Biological Sciences Division at the University of Chicago is seeking a Clinical Research Coordinator I to support clinical studies. The role involves coordinating trial aspects, ensuring compliance with regulations, and managing patient schedules. The minimum requirement...Work at office$29.36 - $42.61 per hour
...expected to be offered for the position. Offers may vary depending on the circumstances of each case. Job Summary: The Clinical Research Coordinator III (CRC III) independently manages the full scope of clinical research study execution for complex, multi-site, or...Hourly payFull timeLocal areaShift work$23.12 - $32.66 per hour
...offered for the position. Offers may vary depending on the circumstances of each case. Summary: Job Summary: The Clinical Research Coordinator I (CRC I) supports the conduct of clinical research studies across a range of disciplines. Receives direction from...Hourly payFull timeLocal areaShift workNight shiftWeekend workAfternoon shift$27.47 - $38.81 per hour
...expected to be offered for the position. Offers may vary depending on the circumstances of each case. Job Summary: The Clinical Research Coordinator II (CRC II) independently coordinates assigned aspects of clinical research studies across a range of disciplines....Hourly payFull timeLocal areaShift workWeekend workAfternoon shift
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