936 Results for

Clinical Research Manager Jobs in Chicago, IL

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New!

Evanston, ILToday

Our more than 25,000 team members and more than 6,000 physicians aim to deliver transformative patient experiences and expert care close to home across more than 300 ambulatory locations and eight acute care hospitals – Edward (Naperville), Elmhurst, Evanston, Glenbrook (Glenview), Highland Park, Northwest Community (Arlington Heights) Skokie and Swedish (Chicago) – all recognized as Magnet hospitals for nursing excellence. Endeavor Health is a fully integrated healthcare delivery system committed to providing access to quality, vibrant, community-connected care, serving an area of more than 4.2 million residents across six northeast Illinois counties.

New!

Evanston, ILToday

Partners with peers and colleagues on the creation and implementation of programs and presentation such as just-in-time education, presentations, and practical skills in clinical and/or simulation setting utilizing evidence-based practice and adult learning theory. • Consults with Nursing Leadership, Clinical Nurse Educators, Department Based Educators and other system teams to establish annual competencies/skill days and other educational needs.

Arlington Heights, IL13 days ago

Our more than 25,000 team members and more than 6,000 physicians aim to deliver transformative patient experiences and expert care close to home across more than 300 ambulatory locations and eight acute care hospitals – Edward (Naperville), Elmhurst, Evanston, Glenbrook (Glenview), Highland Park, Northwest Community (Arlington Heights) Skokie and Swedish (Chicago) – all recognized as Magnet hospitals for nursing excellence. • Partners with peers and colleagues on the creation and implementation of system continuing education programs and presentations, such as professional role development, practical skills in clinical and/or simulation setting utilizing evidence-based practice and adult learning theory.

New!

Glenview, ILToday

Our more than 25,000 team members and more than 6,000 physicians aim to deliver transformative patient experiences and expert care close to home across more than 300 ambulatory locations and eight acute care hospitals – Edward (Naperville), Elmhurst, Evanston, Glenbrook (Glenview), Highland Park, Northwest Community (Arlington Heights) Skokie and Swedish (Chicago) – all recognized as Magnet hospitals for nursing excellence. This leadership role is primarily responsible for coordinating and facilitating structures and processes that support external nursing students pursing clinical experiences at Endeavor Health for undergraduate and graduate nursing degrees.

Evanston, IL13 days ago

Our more than 25,000 team members and more than 6,000 physicians aim to deliver transformative patient experiences and expert care close to home across more than 300 ambulatory locations and eight acute care hospitals – Edward (Naperville), Elmhurst, Evanston, Glenbrook (Glenview), Highland Park, Northwest Community (Arlington Heights) Skokie and Swedish (Chicago) – all recognized as Magnet hospitals for nursing excellence. Manage education and training processes/activities to foster learning using strategies that engage learners in critical inquiry, critical thinking, problem solving, and foster the development of competence in learners.

New!

Evanston, ILToday

Our more than 25,000 team members and more than 6,000 physicians aim to deliver transformative patient experiences and expert care close to home across more than 300 ambulatory locations and eight acute care hospitals – Edward (Naperville), Elmhurst, Evanston, Glenbrook (Glenview), Highland Park, Northwest Community (Arlington Heights) Skokie and Swedish (Chicago) – all recognized as Magnet hospitals for nursing excellence. Manage education and training processes/activities to foster learning using strategies that engage learners in critical inquiry, critical thinking, problem solving, and foster the development of competence in learners.

New!

Arlington Heights, ILToday

Our more than 25,000 team members and more than 6,000 physicians aim to deliver transformative patient experiences and expert care close to home across more than 300 ambulatory locations and eight acute care hospitals – Edward (Naperville), Elmhurst, Evanston, Glenbrook (Glenview), Highland Park, Northwest Community (Arlington Heights) Skokie and Swedish (Chicago) – all recognized as Magnet hospitals for nursing excellence. • Partners with peers and colleagues on the creation and implementation of programs and presentation such as just-in-time education, presentations, and practical skills in clinical and/or simulation setting utilizing evidence-based practice and adult learning theory.

New!

Chicago, ILToday

New!

Chicago, ILToday

Chicago, IL13 days ago

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

$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.

Chicago, Illinois30+ days ago

Chicago, IL11 days ago

Manager Clinical Research - Anatomy & Cell Biology - Full-time - Rush University Medical Center.

Chicago, IL30+ days ago

$83,200–$137,280 Per Year

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. There's a Place for You with Us: 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, 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.

Hyde Park, IL30+ days ago

$120,000–$170,000 Per Year

Operating within a matrixed academic medical center environment, this role partners closely with senior academic and hospital leadership, faculty investigators, and multidisciplinary technical teams to ensure clinical data are transformed into trusted, interoperable, and AI-ready research assets. This role is intentionally designed as a hybrid management position: the Manager is accountable for strategy, architecture, prioritization, team leadership, and optimization of technical solutions, while generally guiding and overseeing implementation rather than serving as the primary individual contributor.

Chicago, Illinois30+ days ago

Lurie Children’s Hospital of Chicago, including 1) coordination of activities for the program including, but not limited to, program meetings and events including development of interdisciplinary colloquium; 2) annual call for research proposals and management of reporting from proposal awardees, 3) oversight of current and future quality and process improvement initiatives developed by program leadership, such as coordination of QI projects (i.e. establishing project charters, timelines and metrics); 4) implementation of community outreach and advocacy efforts that benefit patients living with Leukemia; 5) partner with leaders to increase visibility of the program, including working with the Marketing team to maintain website and advertising and development team to collaborate with program donors, and 6) prepare and disseminate quarterly reports for program donors. The Program Manager will work closely with program leaders to build and grow the Cal’s Angels Advanced Leukemia and Research Program through developing and nurturing partnerships with referring providers and external physicians participating in the program’s tumor board.

Chicago, IL30+ days ago

$70,720–$115,627.20 Per Year

Lurie Childrens Hospital of Chicago, including 1) coordination of activities for the program including, but not limited to, program meetings and events including development of interdisciplinary colloquium; 2) annual call for research proposals and management of reporting from proposal awardees, 3) oversight of current and future quality and process improvement initiatives developed by program leadership, such as coordination of QI projects (i.e. establishing project charters, timelines and metrics); 4) implementation of community outreach and advocacy efforts that benefit patients living with Leukemia; 5) partner with leaders to increase visibility of the program, including working with the Marketing team to maintain website and advertising and development team to collaborate with program donors, and 6) prepare and disseminate quarterly reports for program donors. The Program Manager will work closely with program leaders to build and grow the Cals Angels Advanced Leukemia and Research Program through developing and nurturing partnerships with referring providers and external physicians participating in the programs tumor board.

Chicago, IL30+ days ago

$60,000–$85,000 Per Year

Act as liaison to funding agencies (NCI CTEP and DCP staff), the Cancer Trials Support Unit (CTSU), and the NCI Central Institutional Review Board (CIRB), regarding studies in development or undergoing revision, and monitor progress of review performed by these organizations. Distribute protocol drafts for review, integrate technical and scientific information from multiple sources and incorporate necessary revisions under the supervision of Alliance Executive Officers and other senior leadership, as necessary.

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.

Hyde Park, IL30+ days ago

$70,000–$100,000 Per Year

These research trials (both established and future) will include multi-centered cooperative group and intergroup trials at a national level, multi-institutional pharmaceutical trials, device trials, and single and multi-centered trials, designed, implemented, and coordinated in the Section. This position will play a central role in the conduct of investigator-initiated and industry-sponsored clinical trials across the cardiovascular service line, including (but not limited to) heart failure, interventional cardiology, electrophysiology, pulmonary hypertension, and device-based therapies.

Chicago, IL30+ days ago

$60,000–$75,000 Per Year

Responsibilities include, but are not limited to, provides efficient and complete data collection, processing, analysis and reporting; assures source documentation and data abstraction and entry are being done at the protocol specified time-points; ensures data accuracy and integrity by working closely with internal monitors and/or auditors to promptly resolve any data quality concerns or outstanding queries; and, facilitates the exchange of data across projects and organizations. Plans and coordinates subjects schedule for study procedures, return visits, and study treatment schedules; educates subjects about study procedures to be performed, what to report between and during visits, and the risks and benefits of the procedures; performs assessments at visits and monitors for adverse events.

Chicago, IL30+ days ago

$40.75–$72.94 Per Hour

Exemplifies the Rush mission, vision and values and acts in accordance with Rush policies and procedures.\n \nOther information:\n \nRequired Job Qualifications:\n\n Education: Bachelor of Science in Nursing (BSN) OR Master of Science in Nursing (MSN)\n Experience: Two years of clinical nursing practice experience required\n Licenses: Current State of Illinois Registered Nurse Licensure\n Certifications: Current Basic Life Support certification for Healthcare Professionals\n \nKnowledge, Skills, and Abilities:\n\n Regulatory Compliance Awareness \u2013 Able to demonstrate introductory knowledge of Good Clinical Practices and/or Good Documentation Practices, human subjects protections, institutional, local, state and federal guidelines and regulations related to clinical research\n Communication Skills \u2013 Ability to communicate complex clinical and regulatory concepts in easy-to-understand language.\n \n Certifications: Clinical specialty certification appropriate to study population\n \nPhysical Demands:\n \nCompetencies:\n \nDisclaimer: The above is intended to describe the general content of and requirements for the performance of this job It is not to be construed as an exhaustive statement of duties, responsibilities or requirements\n \nResponsibilities:\n \nJJob Responsibilities:\n \nRelationships and Caring\n\n Delivers protocol-required nursing care to research participants, including monitoring of health status and documentation \n Follows participant care plans based on protocol requirements and participant needs\n Assesses participant status and communicates follow-up needs to the PI or interdisciplinary care team in alignment with protocol \n Communicates study details and updates to participants, families, and interdisciplinary care team members\n Educates interdisciplinary care teams on protocol requirements \n Notifies the PI and care team of changes in participant health status.\n

Oak Forest, Illinois30+ days ago

$21–$23.50 Per Hour

Position Summary: We are now hiring for a Clinical Research Assistant that will support a high-volume Resarch Department within an ophthalmic practice that focuses on providing quality and compassionate care to each patient needed complete eye care services. The physicians diagnose and treat retinal-related conditions, including macular degeneration, diabetic retinopathy, retinal detachment repair, and other disorders of the retina, vitreous, and macula.

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.

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, 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, Illinois12 days ago

The Research Financial Portfolio Manager, Sr will serve as lead subject expert regarding Lurie Children’s and Stanley Manne Children’s Research Institute post-award policies, procedures and systems and assist with management of the finances of the sponsored projects for assigned Departments, Divisions and PIs. Minimum of five years of work experience involving grant/research administration, combined with experience with legal terminology, reviewing detailed legal documents, and language relevant to award administration, and/or accounting related experience to include tracking and reconciling accounts.

Chicago, Illinois30+ days ago

The Research Financial Portfolio Manager will serve as lead subject expert regarding Lurie Children’s and Stanley Manne Children’s Research Institute post-award policies, procedures and systems and assist with management of the finances of the sponsored projects for assigned Departments, Divisions and PIs. Minimum of five years of work experience involving grant/research administration, combined with experience with legal terminology, reviewing detailed legal documents, and language relevant to award administration, and/or accounting related experience to include tracking and reconciling accounts.

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.

New!

Chicago, Illinois5 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. Collects specimens from subjects and ensures proper processing, records data on source documents and electronic systems, and conducts literature searches while assisting with QA/QC procedures to ensure data accuracy and protocol compliance.

Chicago, Illinois30+ days ago

Chicago, Illinois17 days ago

Chicago, IL30+ days ago

Requirement : • Bachelors and/or a combination of related experience • 8+ years' experience • Able to handle a variety of clinical research tasks • Excellent organizational and communication skills • Professional use of the English language; both written and oral • Experience in utilizing various clinical database management systems • Broad knowledge of drug, device and/or biologic development and effective data management practices • Strong representational skills, ability to communicate effectively orally and in writing • Strong leadership and interpersonal skills • Systems knowledge with Medidata Rave and Veeva • Ability to undertake occasional travel. • Develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders • May assist in building clinical databases • Conduct database build UAT and maintain quality controlled database build documentation.

Libertyville, IL27 days ago

$44.15–$66.25 Per Hour

Must demonstrate knowledge of the principles of growth and development over the life span and possess the ability to assess data reflective of the patient's status and interpret the appropriate information needed to identify each patient's requirements relative to his/her age-specific needs, and to provide the care needed as described in the department's policies and procedures. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with Wake Forest University School of Medicine serving as the academic core of the enterprise.

Hyde Park, IL14 days ago

$60,000–$75,000 Per Year

Chicago, 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, IL12 days ago

$19.23–$24.04 Per Hour

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. The Office of Clinical Research (OCR) is the nucleus of the clinical research enterprise, providing services, training, tools and compliance oversight to support the conduct of clinical research across the entire Biological Sciences Division and University of Chicago Medicine human subject research portfolio.

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.

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, 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.

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.

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, 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.).

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.

Hyde Park, IL30+ days ago

$75,000–$100,000 Per Year

The Office of Clinical Research (OCR) is dedicated to supporting the infrastructure for the management and administration of clinical research at The University of Chicago as well as individual research programs with the goal of improving communication, consistency and collaboration across the Biological Sciences Division and UChicago Medicine. The mission of the OCR 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.

Chicago, IL30+ days ago

$50,000–$65,000 Per Year

Under the supervision of the Technical Director and facility manager of the cGMP Core, this position requires the candidate to collaborate within a team atmosphere that process and compound clinical grade vaccines and cell therapy products in the Cellular and Tissue Based Processing cGMP Facility. This registration complies with federal regulations that require clinical facilities engaged in production of cellular products follow strict guidelines to minimize microbial contamination and manufacture cellular-based products that are sterile and potent for their intended purpose.

Hyde Park, IL12 days ago

$50,000–$65,000 Per Year

The Section provides extremely valuable collaborations with investigators in the Department of Medicine who are seeking to develop new and more powerful ways to identify genetic risk factors for common, complex disorders with almost immediate clinical application. Facilitates and participates in the daily activities of moderately complex clinical studies and performs various activities including patient data retrieval, documenting clinical research records, and participation in program audits.

Chicago, IL30+ days ago

Duties and Responsibilities Planning and implementation clinical trial to include but not limited to: • Coordination with all members departments external institutions of the study team • Oversight of IRB regulatory and/or FDA submissions • Budget preparation • Participation and study management • Tool development • Provide education and training to other health care professionals related to patient participation in a clinical trial • Screening, recruitment, and enrollment of study participants • Procure eligibility data and materials • Interface with sponsors, investigators as appropriate in determining eligibility • Oversee study lab specimen collection, processing, and shipping, and long-term data collection • Prepare and participate in Cooperative Group Audits • NCI FDA Sponsor GCP quality audits • Loyola internal audits and department audits • Participation in program research planning to include as appropriate: • Protocol development • Data reporting • Grant reporting • Participate in Departmental Process Improvement Activities • National Committees as appropriate • Collaborates with the PI in the case management of protocol patients, assuring patient safety and compliance with the protocol and regulatory requirements and patient billing compliance • Communicates with the appropriate clinical staff in coordination of patient care • Data management, collecting data entry of accurate data • Monitor and train clinical protocol coordinators in accurate and timely data collection • Provide oversight and guidance to clinical protocol coordinators regarding several research protocols • IRB submissions and regulatory management • Perform other duties as assigned. Minimum Education and/or Work Experience Minimum Education Required: Bachelors Degree OR equivalent training acquired via work experience or education Preferred Bachelors Degree Specify Degrees Nursing Minimum Experience Required: 1-2 years of previous job-related experience Preferred 3-5 years of previous job-related experience.

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Clinical Research Manager Jobs in Chicago, IL

Clinical Nurse Manager-Cardiac/Stroke/Tele Endeavor Health

RN Clinical Nurse Practice Specialist Endeavor Health

Clinical Nurse Educator - Days Endeavor Health

Program Manager, Nursing Academic Affiliations Endeavor Health

Clinical Nurse Educator - Unit Based - 4L Med/Surge/Overflow - Days Endeavor Health

Clinical Nurse Educator-Department Based - 2L Med-Surg/Stroke/Tele - Days Endeavor Health

RN Clinical Nurse Practice Specialist - Critical Care - Days Endeavor Health

RN - Resource Team - Days/Nights Endeavor Health

RN Resource Team - Rotating Days/Nights Endeavor Health

RN Resource Team - Nights Endeavor Health

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

Clinical Research Manager, Research Incubation Unit University of Chicago

Manager Clinical Research (Center for Cancer and Blood Disorders) Ann & Robert H. Lurie Children's Hospital of Chicago

Manager Clinical Research - Anatomy & Cell Biology - Full-time Rush University Medical Center

Manager Clinical Research (Center for Cancer and Blood Disorders) Ann & Robert H Lurie Children's Hospital of Chicago

Clinical Research Project Manager Northwestern University

Manager of Clinical Research Data Warehousing University of Chicago

Program Manager – Advanced Leukemia Clinical and Research Program Ann & Robert H. Lurie Children's Hospital of Chicago

Program Manager - Advanced Leukemia Clinical and Research Program Ann & Robert H Lurie Children's Hospital of Chicago

Clinical Trials Manager University of Chicago

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

Clinical Research Nurse University of Chicago

Clinical Research Coordinator 2, Transplant Surgery University of Chicago

Clinical Research Nurse 1 - Cancer Research Rush University Medical Center

Clinical Research Assistant University Retina

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

Clinical Research Coordinator II Iterative Scopes Inc

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

Sr. Research Financial Portfolio Manager Ann & Robert H. Lurie Children's Hospital of Chicago

Research Financial Portfolio Manager - 32321 Ann & Robert H. Lurie Children's Hospital of Chicago

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

Clinical Research Coordinator II-Pulmonary and Sleep Medicine Ann & Robert H. Lurie Children's Hospital of Chicago

Clinical Research Coordinator II-Nephrology 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

Senior Clinical Data Manager Precision Medicine Group LLC

Assistant Clinical Manager Neuro Complex Medical Advocate Aurora Health Inc

Clinical Research Coordinator 2, Department of Surgery University of Chicago

Clinical Research Associate, Sponsor Dedicated IQVIA Holdings Inc

Clinical Research Assistant University of Chicago

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

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

Temporary Clinical Research Nurse Coordinator, Clinical Trials University of Chicago

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

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

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

Clinical Research Coordinator I Ora Inc

Clinical Trial Budget/Contract Manager University of Chicago

Clinical Research Coordinator 1 University of Chicago

Clinical Research Coordinator I University of Chicago

Clinical Research Nurse Loyola University Chicago

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