363 Results for

Clinical Research Associate Jobs in Chicago, IL

Jobs

New!

Chicago, IL1 day ago

The RUSH Section of Sleep Surgery provides comprehensive care for patients with sleep disorders, offering the full spectrum of procedures, including nasal and soft tissue surgery, hypoglossal nerve stimulation and skeletal procedures, such as maxillomandibular advancement surgery and surgically-assisted rapid palatal expansion. The total pay range shown reflects the wide range of factors that are considered in making compensation decisions including, but not limited to, knowledge and skills; relevant experience and training; education, certifications, and licensure; primary work location; and other business and organizational factors.

New!

Chicago, IL1 day ago

The total pay range shown reflects the wide range of factors that are considered in making compensation decisions including, but not limited to, knowledge and skills; relevant experience and training; education, certifications, and licensure; primary work location; and other business and organizational factors. Rush University Medical Center, a nationally recognized clinical and academic institution and the teaching hospital for Rush Medical and Nursing Colleges, invites applications for the positions of Endourologist and Urologist-Men’s Health in the Department of Urology.

New!

Chicago, IL1 day ago

Chicago, IL The Division of Geriatric Medicine and Palliative Care at Rush University Medical Center, a nationally recognized clinical and academic institution and the teaching hospital for Rush Medical and Nursing Colleges, invites applications from exceptional clinicians for a full-time Geriatric Medicine Faculty position at the Assistant or Associate Professor level. The total pay range shown reflects the wide range of factors that are considered in making compensation decisions including, but not limited to, knowledge and skills; relevant experience and training; education, certifications, and licensure; primary work location; and other business and organizational factors.

Chicago, IL11 days ago

Clinical Trial Monitoring: Conduct site qualification, site initiation, interim monitoring, and close-out visits to ensure compliance with the study protocol, Good Clinical Practice (GCP), and regulatory guidelines. As a Clinical Research Associate II (CRA II) specializing in oncology, you will play a crucial role in the execution and management of Phase 1, Phase 2, and Phase 3 clinical trials.

Chicago, IL30+ days ago

$112,154.40–$168,231.60 Per Year

In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). The CRA is responsible for the preparation, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with AZ Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the.

New!

IL5 days ago

Remote

$97,000–$193,000 Per Year

Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.

Downers Grove, IL30+ days ago

Remote

Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.

New!

Chicago, Illinois4 days ago

What You’ll Do: • Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.

Chicago, IL23 days ago

Remote

$120,000–$135,000 Per Year

The Clinical Research Associate will function as the primary bridge between sponsors and sites, ensuring clinical trials follow protocols, protect patients, and meet all regulatory expectations to succesffuly create lifesaving drugs and treatments. Piper Companies is actively seeking Clinical Research Associates to join a top‑tier CRO with a proven track record of excellence, trusted by global pharma and biotech partners.

Chicago, IL30 days ago

$49,850–$69,000 Per Year

The available benefits package for this position will include health, dental, vision, disability, and life insurance; paid vacation and holidays; paid medical/sick and parental leave; tuition benefits for the employee and dependents; pre-tax and flex spending accounts for commuting and dependent care; generous retirement savings options; and wellness programs. 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 with regulatory laws and institutional guidelines.

Chicago, IL11 days ago

Remote

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Companys sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.

Chicago, IL19 days ago

Willing and able to travel up to 60% for on-site monitoring visits across the Midwest region; preference given to candidates residing in Midwest region near major HUB airports to support efficient regional travel. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

Orland Park, IL30+ days ago

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.

Chicago, IL30+ days ago

$91,336–$114,170 Per Year

Willing and able to travel up to 50% for on-site monitoring visits across southeast region; preference given to candidates residing in Chicago near major HUB airports to support efficient regional travel. Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Chicago, IL30+ days ago

What Youll Do: Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.

Chicago, Illinois30+ days ago

Chicago, IL25 days ago

Remote

$85–$90 Per Hour

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. The role offers a weekly workload of 40-50 hours, varying by study phase, with opportunities for hybrid work arrangements to support work-life balance.

Chicago, IL30+ days ago

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Chicago, IL30+ days ago

$115,500–$204,600 Per Year

Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). CRLs partner closely with internal Lilly teams (including Clinical Development and Medical Affairs) to ensure that insights from the field shape development strategies and that development strategies are delivered with operational excellence and scientific clarity.

Chicago, IL30+ days ago

With 15 schools, colleges, and institutes-including Business, Law, Medicine, Nursing, and Health Sciences-Loyola operates three primary campuses in the greater Chicago area and one in Rome, Italy, that provide students a transformative, globally connected learning experience. No Job Category University Staff Job Type Full-Time FLSA Status Non-Exempt Campus Maywood-Health Sciences Campus Department Name RADIATION ONCOLOGY Location Code RADIATION ONCOLOGY (06720A) Is this split and/or fully grant funded?

Riverside, Illinois30+ days ago

The primary function of the Clinical Research Coordinator (CRC) is to coordinate the conduct of clinical research studies in a clinic/hospital setting with an emphasis on the screening, enrollment, and monitoring of research patients. As an integrated health system, we deliver exceptional, coordinated across seven hospitals, 85 primary and specialty clinics, and a team of over 7,500 professionals serving northern Illinois and southern Wisconsin.

Munster, Indiana30+ days ago

Our Mission: Improving Lives by Providing Advanced Therapeutic Options Our Vision: Creating the Absolute Best Patient-Physician Experience in Clinical Research Our Values: Compassion: We prioritize the patient-physician relationship, ensuring every interaction is service-oriented and patient-centered. You’ll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs.

Chicago, IL9 days ago

Maintains research files, designs forms as needed, reports findings as appropriate, assists in preparation or review of material for submission to an IRB including reviewing and editing protocols and consent documents, where applicable. Attends investigator's meetings, coordinates and attends pre-study site visits, study initiation visits, and all other study-related visits by Monitors or Sponsor representatives, when required.

Chicago, Illinois30+ days ago

The Clinical Research Quality Assurance and Improvement (QA/QI) Specialist utilizes knowledge to 1) analyze and interpret applicable regulations, 2) develop/revise institutional policies and procedures, 3) audit the conduct of human subjects research (biomedical, social & behavioral) and research oversight programs, 4) assess compliance with all applicable regulations, guidances, and policies and procedures, 5) identify areas of risk, and 6) oversee the development and implementation of corrective and preventive action plans. 4. Certification or eligibility to sit for Certification Exam in relevant area (i.e., Certified IRB Professional (PRIM&R), Certified Clinical Research Professional (SOCRA), Certified Clinical Research Coordinator or Associate (ACRP), Society for Quality Assurance and the American Society for Quality, etc.).

Des Plaines, IL30+ days ago

By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. • Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies.

Chicago, Illinois30+ days ago

Manages participant engagement throughout clinical trials by identifying eligible subjects, conducting informed consent processes, coordinating reimbursement, verifying eligibility, and serving as the primary patient liaison for study-related inquiries and support. At Lurie Children’s, we embrace and celebrate building a team with a variety of backgrounds, skills, and viewpoints — recognizing that different life experiences strengthen our workplace and the care we provide to the Chicago community and beyond.

Chicago, Illinois17 days ago

Chicago, Illinois30+ days ago

At Lurie Children’s, we embrace and celebrate building a team with a variety of backgrounds, skills, and viewpoints — recognizing that different life experiences strengthen our workplace and the care we provide to the Chicago community and beyond. Supports research activities by conducting literature searches, assisting with QA/AC procedures, entering, coding, creating, updating data spreadsheets, retrieving, preparing, and managing data through importing and exporting in various formats.

Chicago, IL30+ days ago

Perform various tasks (post-onboarding) such as use of proprietary technology, performing the Informed Consent process, documenting medical history and medications, taking vitals, scribing for medical staff, dispensing study drug, performing allergy skin tests, documenting controlled environment stats, and other ophthalmic assessments. Our CRC I's will partner with tenured Clinical Research Coordinators and Clinical Project Managers to execute protocol directives and work cross-functionally with internal and external teams such as other Research Coordinators and Investigators.

Chicago, IL30+ days ago

The Clinical Research Nurse Coordinator is a registered professional nurse who demonstrates exemplary clinical research knowledge, has strong communication skills, and is responsible for serving as a liaison between Northwestern University (NU) clinical research investigator teams and Northwestern Medicine; a joint collaboration between NMG and the NU Feinberg School of Medicine. Collaborate with a wide range of professionals to disseminate patient care outcomes through publications and presentations, managing all stages of research projects-from feasibility, project conception and approval, data collection, literature review to manuscript submission.

New!

Chicago, IL4 days ago

$25–$31.50 Per Hour

The multidisciplinary team includes board-certified physicians, licensed clinicians, psychometricians, and experienced research professionals who collaborate closely on studies across psychiatric, sleep, psychedelics, vaccine, cardiometabolic, and general medicine indications. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Hyde Park, IL30+ days ago

$50,000–$65,000 Per Year

The 30 faculty, clinical associates and research associates along with a staff of more than 72 have devoted themselves to the pursuit of excellence in each of these important activities.\n \nThe MICU Research Program, with Dr. Krysta Wolfe is looking for a dedicated research coordinator to aid with the development/maintenance of datasets and data collection for a variety of projects related to the care of patients in the intensive care unit.\n \nJob Summary\n \nThe Clinical Research Coordinator I (CRC I) provides support to the faculty of the Section of Pulmonary/Critical Care within the Department of Medicine. \n\n \nPreferred Competencies\n\n Ability to interact and communicate with clarity, tact, and courtesy with patrons, patients, staff, faculty, students, and others.\n \n\n Ability to communicate with tact and diplomacy.\n \n\n Strong organizational skills.\n \n\n Strong communication skills (verbal and written).\n \n\n Excellent interpersonal skills.\n \n\n Strong data management skills and attention to detail.\n

Chicago, IL30+ days ago

$70,720–$115,627.20 Per Year

The Clinical Research Quality Assurance and Improvement (QA/QI) Specialist utilizes knowledge to 1) analyze and interpret applicable regulations, 2) develop/revise institutional policies and procedures, 3) audit the conduct of human subjects research (biomedical, social & behavioral) and research oversight programs, 4) assess compliance with all applicable regulations, guidances, and policies and procedures, 5) identify areas of risk, and 6) oversee the development and implementation of corrective and preventive action plans. Certification or eligibility to sit for Certification Exam in relevant area (i.e., Certified IRB Professional (PRIM&R), Certified Clinical Research Professional (SOCRA), Certified Clinical Research Coordinator or Associate (ACRP), Society for Quality Assurance and the American Society for Quality, etc.).

Chicago, IL14 days ago

$49,920–$81,619.20 Per Year

Essential Job Functions: Coordinates and manages the initiation and regulatory compliance of clinical research studies, including preparing all necessary documents for IRB and sponsor review, coordinating study conduct across departments, and securing required approvals. Manages participant engagement throughout clinical trials by identifying eligible subjects, conducting informed consent processes, coordinating reimbursement, verifying eligibility, and serving as the primary patient liaison for study-related inquiries and support.

Chicago, IL30+ days ago

$46,280–$75,670.40 Per Year

At Lurie Children's, we embrace and celebrate building a team with a variety of backgrounds, skills, and viewpoints - recognizing that different life experiences strengthen our workplace and the care we provide to the Chicago community and beyond. Supports research activities by conducting literature searches, assisting with QA/AC procedures, entering, coding, creating, updating data spreadsheets, retrieving, preparing, and managing data through importing and exporting in various formats.

Orland Park, IL30+ days ago

$70,000–$85,000 Per Year

While the Principal Investigator is primarily responsible for the overall design, conduct, and management of clinical trials, the Sr CRC oversees, facilitates, and coordinates the daily activities of complex clinical trials and plays a critical role in their conduct to ensure compliance with federal and institutional regulations. The Comprehensive Cancer Center comprises over 200 faculty members from twenty departments, with members currently being awarded over $51million in total direct costs in peer-reviewed cancer research grants, and $24 million in non-peer-reviewed grants and contracts.

Chicago, IL30+ days ago

$31.25–$36 Per Hour

Under the direction of the PI, Co-Investigators, Advanced Practice Registered Nurses (APRNs) and Research Manager (RM), the Clinical Research Nurse Coordinator oversees, facilitates, and participates in the conduct of daily activities of complex clinical trials and plays a critical role in the conduct of the studies to ensure compliance with federal and institutional regulations. The Institute for Population and Precision Health (IPPH), located in the Biological Sciences Division, integrates a wide spectrum of factors such as human health behaviors, environmental factors, social and economic factors, policies and genetic determinants of health, into studies focused on the treatment and prevention of disease, as well as the maintenance of wellness.

Hyde Park, IL30+ days ago

$60,000–$75,000 Per Year

Analyzes, facilitates and participates in the daily activities of multiple moderately complex clinical trials and performs all aspects of clinical data management, including patient data retrieval, referring MD office records, preparing clinical research charts, and participation in program audits. The Medical Intensive Care Unit (MICU) Research Program, is looking for a Clinical Research Coordinator II to aid with the development/maintenance of datasets and data collection for a variety of projects related to the care of patients in the intensive care unit.

Chicago, Illinois30+ days ago

Works with the Research Business Operations (RBO) offices and Office of Clinical and Community Trials (OCCT) to facilitate contract negotiations and execution, to ensure proper accrual tracking, and to provide additional information as needed for timely financial reconciliation, management, and reporting. In conjunction with the SMCRI central offices; monitors study funds, reconciling faculty and staff salaries, subcontractor invoices, incoming sponsor payments, cost transfers and other allocable expenses ensuring financial compliance.

Chicago, IL30+ days ago

Clinical Research Coordinator III - Emergency Medicine Clinical Trials - Rush University Medical Center.

Chicago, IL30+ days ago

$50,000–$65,000 Per Year

In addition to CRC1, the position will also serve as a Dental Assistant (DA1) at The University of Chicago Medicine (UCM) Dental Research Study Clinic and will be responsible for chairside assisting to dental providers providing dental care to patients at the University of Chicago Medicine (UCM) Dental Research Study Clinic at its main campus in Hyde Park as well as other study sites, including mobile dental units. The Clinical Research Coordinator I - Oral Health Research Staff (CRCI) is an entry level researcher working with the Principal Investigator (PI) Dr. David Meltzer, Co-Investigator(s) and other study personnel, to support and provide guidance on the administration of the compliance, financial and other related aspects of the clinical study.

Chicago, IL30 days ago

$65,000–$79,500 Per Year

Oversees day-to-day operations including identifying & securing needed resources; creating, implementing, monitoring, & updating project plans; facilitating meetings with appropriate parties; tracking tasks/deliverables to ensure timelines, milestones &/or goals are attained; monitoring & reporting progress as appropriate; & resolving or escalating issues in a timely manner. Collaborating with nursing staff and Principal Investigator (PI) ascertains pretreatment & eligibility requirements; interviews participants & obtains social & medical histories; based on results determines & registers participants with appropriate sponsors; completes informed consent; determines & organizes patients treatment and test schedules.

Chicago, IL30+ days ago

$90,000–$130,000 Per Year

The Clinical Research Incubation Unit was established to enable growth of clinical research portfolios across the Biological Sciences Division as well as provide timely research staffing services to departments or units in need of short-term clinical research management services. The mission of the Office of Clinical Research is to catalyze clinical research by providing expertise, resources, infrastructure, and systems that facilitate clinical research operations and enable collaboration across the enterprise while promoting compliance and human subject protection on behalf of our diverse community of patients and volunteers.

Munster, IN30+ days ago

Lead, implement and coordinate duties for assigned clinical trials including but not limited to study start up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, management and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow up. Ensure good documentation practices are applied by all team members when collecting, maintaining and correcting study data and required records of clinical trial activity including but not limited to source documentation, case report forms, queries, drug dispensation records, and regulatory forms.

Chicago, IL26 days ago

Remote

$80,000–$105,000 Per Year

At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy. Logs/complete information on sponsor systems and ensures all information provided is accurate (i.e., case report forms, EDC, etc.) and ensures it is completed within timeframe.

Des Plaines, IL30+ days ago

$35–$45 Per Hour

By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need. Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies.

Chicago, IL14 days ago

Assist physicians and clinical staff in the identification of prospective participants.x000d • Assist with outreach to and liaison with staff at community events, contribute to presentations aimed at participant recruitment.x000d • Screen participants for relevant and applicable studies. x000d • Ensure that participant enrollment and research activities comply with established protocols.x000d • Maintain detailed records of results and prepare written reports, including vitals and measurements, and document and convey adverse events.x000d

Chicago, IL12 days ago

Senior Clinical Research Coordinators are responsible for recruiting and retaining participants; developing and implementing SOPs, workflows, and protocol training; allocating staff time and tasks; reviewing data for accuracy; and achieving recruitment and visit completion targets to ensure study objectives are met. The incumbent serves as the primary liaison for the project team, which may include physicians, nurses, project managers, lab technicians, and data staff; and communicates with internal and external hubs, sponsors, national groups and other external entities.

New!

Chicago, IL4 days ago

$19–$44 Per Hour

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. As a Clinical Research Assistant, PRN (Registered Nurse), you'll play a key role in delivering life-changing research opportunities to participants but with the flexibility to work when and where it fits your life.

Chicago, IL30+ days ago

Position Details Position Details Job Title: Clinical Research Coordinator I Position Number: 8151017 Work Modality: Hybrid - 4 In-Person Job Category: University Staff Job Type: Full-Time FLSA Status: Non-Exempt Campus: Maywood-Health Sciences Campus Department Name: CBCC Research Location Code: HEMATOLOGY - ONCOLOGY 06508A. With 15 schools, colleges, and institutes-including Business, Law, Medicine, Nursing, and Health Sciences-Loyola operates three primary campuses in the greater Chicago area and one in Rome, Italy, that provide students a transformative, globally connected learning experience.

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Clinical Research Associate Jobs in Chicago, IL

Sleep Surgeon - Clinical Faculty/Physician Rush University Medical Center

Urology - Endourologist and Men’s Health - Clinical Faculty/Physicians Rush University Medical Center

Geriatric Medicine - Clinical Faculty Rush University Medical Center

Clinical Research Associate II - Chicago, Midwest Perspective Therapeutics Inc

Clinical Research Associate - Cell Therapy - Chicago, IL AstraZeneca Plc

Senior Clinical Research Associate - CNS/Rare Disease - Midwest - Remote Worldwide Clinical Trials Holdings Inc

Senior Clinical Research Associate ICON Plc

Clinical Research Associate II - Oncology, Ophthalmology & Neurology - Central US Thermo Fisher Scientific

Clinical Research Associate Zp Group Llc

Clinical Research Coordinator Associate FSM/CC Northwestern University

Clinical Research Associate II - Neuro & Immunology Remote US - Multiple Openings AbbVie Inc

Clinical Research Associate ICON Plc

Clinical Research Associate, Sponsor Dedicated IQVIA Holdings Inc

Clinical Research Associate II ICON Plc

Clinical Research Associate II - Central/West - Oncology, Ophthalmology Thermo Fisher Scientific Inc

Clinical Research Associate II IRE

Clinical Research Associate Actalent Inc

Sr. Clinical Research Associate, IQVIA IQVIA Holdings Inc

Associate Director, Clinical Research Lead (East Coast/Midwest) Eli Lilly and Co

Clinical Research Coordinator I (IITs) Loyola University Chicago

Oncology Clinical Research Coordinator Rockford Health Physicians

Clinical Research Coordinator- Neurology or Cardiology (Munster, IN) Profound Research

Clinical Research Coordinator - Ophthalmology Northwestern Memorial HealthCare

Clinical Research Quality Assurance and Improvement Specialist Ann & Robert H. Lurie Children's Hospital of Chicago

Clinical Research Coordinator II Iterative Scopes Inc

Clinical Research Coordinator II (Infectious Disease) Ann & Robert H. Lurie Children's Hospital of Chicago

Clinical Research Coordinator II (Infectious Disease/Pathology & Laboratory Medicine) Ann & Robert H. Lurie Children's Hospital of Chicago

Clinical Research Coordinator I-Epilepsy Ann & Robert H. Lurie Children's Hospital of Chicago

Clinical Research Coordinator I Ora Inc

Registered Nurse Clinical Research Nurse Coordinator-Bluhm Cardiovascular Institute Full-time Days Northwestern Memorial HealthCare

Clinical Research Coordinator Actalent Inc

Clinical Research Coordinator I University of Chicago

Clinical Research Quality Assurance and Improvement Specialist Ann & Robert H Lurie Children's Hospital of Chicago

Clinical Research Coordinator II (Infectious Disease/Pathology & Laboratory Medicine) Ann & Robert H Lurie Children's Hospital of Chicago

Clinical Research Coordinator I-Epilepsy Ann & Robert H Lurie Children's Hospital of Chicago

Sr. Clinical Research Coordinator University of Chicago

Temporary Clinical Research Nurse Coordinator, Clinical Trials University of Chicago

Clinical Research Coordinator II University of Chicago

Clinical Research Manager (Infectious Disease & Pathology/Laboratory Medicine) Ann & Robert H. Lurie Children's Hospital of Chicago

Clinical Research Coordinator III - Emergency Medicine Clinical Trials Rush University Medical Center

Clinical Research Coordinator I - Oral Health Research Staff University of Chicago

Clinical Research Project Manager Northwestern University

Clinical Research Manager, Research Incubation Unit University of Chicago

Clinical Research Coordinator- Neurology or Cardiology (Munster, IN) Profound Research LLC

Traveling Clinical Research Coordinator II Thermo Fisher Scientific Inc

Senior Clinical Research Coordinator Iterative Scopes Inc

Visiting Clinical Research Coordinator - Department of Medicine, Division of Breathe Chicago Center University of Illinois at Chicago

Visiting Senior Clinical Research Coordinator - Dept of Medicine, Division of Breathe Chicago Center University of Illinois at Chicago

Clinical Research Assistant, PRN (Phlebotomist, LVN or Registered Nurse) Care Access

Clinical Research Coordinator I Loyola University Chicago

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