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
$28 per hour
...Position Details Position Details Job Title CLINICAL RESEARCH COORDINATOR I Position Number 8151017 Work Modality Hybrid - 4 In-Person Is this request for the creation of a new Position (or the modification of an existing...SuggestedHourly payFull timeWork experience placementWork at officeLocal area- ...Robert H. Lurie Children’s Hospital of Chicago is seeking a Clinical Research Support role to assist investigators and study teams in... ...regulatory documentation, protocol preparation, and participant coordination. The position emphasizes adherence to FDA/HSR/GCP...Suggested
$29.95 per hour
...Howard Brown Health Clinical Research CoordinatorHoward Brown Health is a nationally recognized leader in LGBTQ+ health and wellness. Our... ...businesses.Pay: $29.95/hourWhat you can expect:The Clinical Research Coordinator position is responsible for supporting clinical research...SuggestedTemporary workWork at officeLocal areaFlexible hours- ...Clinical Research Coordinator IThe Section of Pulmonary/Critical Care has been a model of exemplary patient care, research and post-doctoral training for more than 20 years. The 30 faculty, clinical associates and research associates along with a staff of more than 72...SuggestedWork experience placement
- ...Ann & Robert H. Lurie Children’s Hospital of Chicago is seeking a Clinical Research Assistant to support investigators and study teams in coordinating and conducting clinical research activities. Under direct supervision, the role balances patient-facing tasks with administrative...Suggested
$31 per hour
...Position Details Position Details Job Title CLINICAL RESEARCH COORDINATOR II Position Number 8150021 Work Modality Hybrid - 4 In-Person Is this request for the creation of a new Position (or the modification of an existing Position) to temporarily...Hourly payFull timeWork experience placementLocal area- Clinical Research Coordinator I Position Title: Clinical Research Coordinator I Position Number: 8151017 Work Modality: Hybrid - 4 In‑Person Job Type: Full‑Time (Non‑Exempt) Campus: Maywood - Health Sciences Department: CBCC Research Job Summary Under the guidance of the...Full timeWork experience placementWork at officeLocal area
- The Clinical Research Coordinator II (Denton, TX) will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. The...
- ...in a friendly, convenient, and compassionate environment. Summary We are seeking a highly motivated and detail-oriented Clinical Research Coordinator to join our growing team. The ideal candidate will play a crucial role in the successful execution of clinical research...Contract work
- Position: Clinical Research Coordinator I Location: Chicago, IL Job Id: 1070 # of Openings: 1 Clinical Research Coordinator I The Clinical Research Coordinator I will ensure that quality research is conducted at the assigned investigative sites in accordance with the...
$60k - $72k
...Job Description Job Description Clinical Research Coordinator in Chicago, IL (60640) Overview: We are seeking a detail-oriented Clinical Research Coordinator to oversee and support all phases of clinical trials involving investigational drugs and medical devices...Local areaMonday to Friday- 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
- Genesis Orthopedics & Sports Medicine is seeking a motivated, organized, and detail-oriented Clinical Research Coordinator to join our growing research department in Oak Brook, Illinois. This is a full-time, on-site position (Monday through Friday, 40 hours per week) with...Full timeMonday to Friday
- Dm Clinical Research Group in Denton, TX seeks a Clinical Research Coordinator II to ensure quality data and adherence to sponsor protocols, FDA regulations and ICH/GCP guidelines. The role emphasizes enrollment targets and timely study conduct across assigned sites. Requirements...
- A leading research university in Chicago is seeking a Clinical Research Coordinator I to manage multiple research protocols, ensuring compliance with clinical guidelines and regulations. The role involves working closely with participants, collecting data, and coordinating...
$46.28k - $75.67k
...latest benefits and innovations in medical technology, research and family-friendly design. As the largest pediatric provider... ...investigators and study team in the implementation, coordination, and conduct of clinical research activities. Adheres to the service values and...Hourly payFull timePart timeFlexible hours$23.12 - $32.66 per hour
...expected to be offered for the position. Offers may vary depending on the circumstances of each case. 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$29.36 - $42.61 per hour
...University Medical Center Department: Pediatric Neurology Research Work Type: Full Time (Total FTE between 0.9 and 1.0... ...of each case. Summary: Job Summary: The Clinical Research Regulatory Coordinator 2 (CRRC 2) prepares, submits, and maintains regulatory...Hourly payFull timeContract workWork at officeShift work- ...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
...the latest benefits and innovations in medical technology, research and family-friendly design. As the largest pediatric provider... .... Location 875 N Michigan (John Hancock) Job Description Coordinates all clinical research activities with moderate supervision. Adheres to the...Flexible hours$60k - $75k
...Clinical Research Coordinator II The Clinical Research Coordinator II (CRCII) is a specialized researcher, partnering with the clinical Principal Investigator (PI) and under the direction of the Clinical Research Manager in the Section of Gastroenterology in the Department...Work experience placementWork at office$51.35k - $60k
...abilities, as well as internal equity and alignment with market data. Job Summary: Coordinates non-therapeutic (i.e., minimal risk, survey, chart review) clinical research protocols with direction from the Principal Investigator and/or senior staff in compliance...Work experience placementWork at office- Genesis Orthopedics & Sports Medicine in Oak Brook, Illinois is seeking a motivated Clinical Research Coordinator for a full-time, on-site position. You'll coordinate clinical trials, manage multiple studies, and support patient care while ensuring protocol compliance....Full time
- NorthShore University HealthSystem is looking for a Research Coordinator - Anesthesia in Evanston, IL. This full-time position involves collaborating... ...infrastructure, assist in protocol development, and manage clinical trials and patient recruitment. The ideal candidate will...Full time
$30 - $38 per hour
Senior Clinical Research Coordinator - Permanent - Chicago, IL Are you ready to make a groundbreaking impact in the world of biotechnology? Join a growing company that's shaping the future of healthcare and science. Proclinical is seeking a Senior Clinical Research Coordinator...Hourly payPermanent employmentPrivate practice$55k - $65k
...Clinical Research Data Coordinator - Cancer Center Clinical Trials Office Search Extension until September 11, 2026 Hiring Department : Clinical Trials Office Location : Chicago, IL USA Requisition ID : 1041069 Posting Close Date : June 12, 2026 Salary...Full timeWork at officeWorldwide$60k - $75k
...considerable institutional strength in population science with research spanning diverse fields such as genetic medicine, cancer... ...differences, such as genetics and metabolism. The Clinical Research Coordinator 2 compiles, documents, analyzes, and reports on clinical...Full timeContract workWork experience placementWork at office- DMCR in Chicago-Melrose Park, IL is seeking a Clinical Research Coordinator to manage site activities for sponsor-led studies, ensuring ICH-GCP and ALCOA-C standards are met. You will train, conduct subject visits, document data, and coordinate with laboratory and data...
- A healthcare research organization is seeking a Clinical Research Coordinator I to manage and ensure compliance for clinical trials. Responsibilities include coordinating studies, managing data collection, and facilitating communication with participants and sponsors....Full time
$70k - $90k
...Visiting Senior Clinical Research Coordinator - Department of Medicine, Breathe Chicago Center Search Extension Until 9/15/2026 Hiring Department :Department of Medicine Location : Chicago, IL Requisition ID :1041393 Posting Close Date : June 19, 2026...Full timeWorldwideShift work
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