73 Results for

Winter Research Jobs in Illinois

Jobs

New!

Peoria, IL4 days ago

$249,084–$351,382 Per Year
Full-time

UICOMP healthcare partners include Jump Simulation, a world-class leader in healthcare simulation and innovation, along with OSF Saint Medical Center, OSF Children’s Hospital of Illinois and Carle Hearth Greater Peoria. The University of Illinois College of Medicine Peoria (UICOMP) seeks candidates for the position(s) of Assistant/Associate/Professor of Clinical Pediatrics (Physical Medicine and Rehabilitation Physician) in the Department of Pediatrics.

Glenview, IL30+ days ago

The company's seven industry-leading segments leverage the unique ITW Business Model to drive solid growth with best-in-class margins and returns in markets where highly innovative, customer-focused solutions are required. Internship Program Overview: ITW's Transfer Pricing internship program provides exposure to the challenging aspects of price determination in relation to related party transactions.

Chicago, IL30+ days ago

Part-time

To better serve our gaming industry clients and focus on the complex issues faced by the industry, we develop our team members to understand the unique operating, regulatory, and financial risks business owners and licensees will face in these gaming markets: Sports Betting Operators. Interns will experience a front row seat to gaming licensee compliance efforts, collaborate with regulators implementing state regulations, and provide advisory services that can help a licensee grow and compete in multiple gaming jurisdictions.

Chicago, IL30+ days ago

Part-time

We leverage our experience with disciplined governance, smart risk management, right-sized control monitoring, internal audit, and business process improvement to help clients operate with greater efficacy and efficiency, comply with regulations, and make better-informed decisions that create lasting value. Compliance Readiness & Assurance: Work closely with your engagement team to support organizations in preparing for and maintaining compliance with crucial regulatory frameworks and industry rules, such as Sarbanes-Oxley (SOX), Anti-money Laundering (AML) laws, Gambling regulations, Banking regulations, Healthcare requirements, Contract compliance, System and Organizational Controls (SOC) and licensing/royalty agreements.

Chicago, IL30+ days ago

$34–$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

$34–$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. Study Operations & Data Management: Accurately document all procedures and results in approved systems (e-source, logs, etc.) according to ALCOA-C++ and ensure regulatory compliance (GxP, HIPAA).

Glenview, IL30+ 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. Benefits (For full time or part time positions): • Opportunity for annual increases based on performance • Career Pathways to Promote Professional Growth and Development • Various Medical, Dental, Pet and Vision options • Tuition Reimbursement • Free Parking • Wellness Program Savings Plan • Health Savings Account Options • Retirement Options with Company Match • Paid Time Off and Holiday Pay • Community Involvement Opportunities.

Chicago, IL30+ days ago

$100,000–$120,000 Per Year

The Clinical Research Associate (CRA) will participate in ongoing Clinical Trials throughout the Country for a leading Clinical Research Organization. Responsibilities for the Clinical Research Associate: Conduct site and study visits and perform all site monitoring activities across multiple study.

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.

PEORIA, Illinois30+ days ago

$62.64–$83 Per Hour

Licensure/ Certification: Research-related certification (Association of Clinical Research Professionals / Certified Clinical Research Coordinator (ACRP/CCRC), Society of Clinical Research Associates / Certified Clinical Research Professional (SOCRA/CCRP), Certified Healthcare Research Compliance (CHRC), Certified in Healthcare Compliance (CHC), etc.) expected within l yr on the job. Additionally, the Director provides expert input on clinical trial budget development, directs local financial and capital planning for research operations, ensures effective oversight of study activation and operational performance, and delivers high-level reporting and communication to the CMO, Research Administration, executive committees, and governing bodies.

Peoria, Illinois9 days ago

$42.64–$56.50 Per Hour

The Manager partners with Research Administration leadership, investigators, nd research teams to identify compliance risks, strengthen research quality, and support the safe and effective conduct of clinical research across the Ministry promoting a culture of quality, participant safety, and regulatory compliance across the OSF research enterprise. This role oversees monitoring and audit activities across active research studies, including early-phase and first-in-human clinical trials, to ensure compliance with federal regulations, Good Clinical Practice (GCP), institutional policies, and approved study protocols.

Chicago, IL30+ days ago

Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family's well-being.

New!

Peoria, IL2 days ago

$39.49–$52.31 Per Hour

Collaborating closely with research administration and various healthcare professionals, you will identify and cultivate opportunities for clinical research, grant programs, and clinical drug trials. As the Manager of Clinical Research, you will have the unique opportunity to lead a multidisciplinary team in conducting Phase I Clinical Oncology trials.

Bedford Park, IL11 days ago

$50,000–$52,000 Per Year

Physical Environment and Requirements Works extensively in a clinical lab environment where there are strong safety procedures protective equipment requirements (wears lab coat, gloves, et)c, and works with various specimens and chemicals <1% May lift up to 10 lbs, 10% of time and performs extensive keyboarding (15%) and pipetting up to 10% of the time. Follows procedures to clean and sterilize lab (kitchen lab and bio-labs) equipment; assists in setting up, adjusting, operating and maintaining equipment and instruments according to procedures.

Peoria, Illinois10 days ago

$38.75–$45.59 Per Hour

POSITION SUMMARY: The Clinical Research Monitor performs monitoring and audit activities across OSF HealthCare’s research portfolio to support institutional oversight of active research studies. OSF HealthCare is dedicated to provide Mission Partners with a comprehensive and market-competitive total rewards package that includes benefits, compensation, recognition and well-being offerings that focus on the whole person and engage with their current stage of life and career.

PEORIA, Illinois30+ days ago

$39.49–$52.31 Per Hour

Experience in research, coding, billing/finance, vendor accounts/relations, EPIC, CTMS, hospital administration, project management, software/database creation and maintenance, customer service, report creation, policy creation/writing, strategic development preferred, Financial Regulations (FDA, OHRP, ORI, DHHS, NIH, CMS), Medicare billing rules, Medicare Clinical Trial Policy. Will be expected to interact with leadership, medical staff and other clinical providers to identify opportunities for clinical research, program grants, and clinical drug trials and match these to the interests of potential investigators, faculty, and departments.

Urbana, Illinois30+ days ago

$63.59–$109.37 Per Hour

The successful applicant will be expected to conceptualize, develop, and lead translational and clinical research projects involving 7T MRI; establish and lead a research group; and establish and sustain an independent externally-funded research program. In addition, the successful applicant will provide leadership and key technical expertise in collaborative imaging research projects among Carle basic science and clinical researchers and with investigators and students at Illinois.

Oak Brook, IL24 days ago

We are looking for candidates with prior clinical research experience who thrive in a fast-paced environment, can independently manage multiple studies, and are passionate about patient care and advancing clinical research. 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.

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.

Peoria, Illinois11 days ago

$62.64–$83 Per Hour

Familiarity with research systems such as, but not limited to, the following: Epic research functionality, CTMS (Clinical Trial Management System), REDCap (Research Electronic Data Capture), iRIS (Integrate Research Information System)/Cayuse. OSF HealthCare is dedicated to provide Mission Partners with a comprehensive and market-competitive total rewards package that includes benefits, compensation, recognition and well-being offerings that focus on the whole person and engage with their current stage of life and career.

Downers Grove, IL30+ days ago

$24.36 Per Hour
Part-time

More than 6,000 full-time students are enrolled in graduate programs in osteopathic medicine, dentistry, pharmacy, physician assistant studies, physical therapy, occupational therapy, nurse anesthesia, cardiovascular perfusion, podiatry, optometry, clinical psychology, speech language pathology, biomedical sciences, and veterinary medicine. Over 500 full-time faculty members and 400 staff members are dedicated to the education and development of our students in an environment that encourages learning, respect for all members of the health care team, service, interdisciplinary scholarly activity, and personal growth.

Chicago, IL30+ days ago

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Chicago, IL30+ days ago

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Moline, IL30+ days ago

Logs/completes 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. " Performs all defined study activities (i.e., informed consent, screening, and protocol procedures which include but not limited to vital signs, pregnancy tests, height, weight, ECG's, etc.).

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

New!

Chicago, IL6 days ago

$19.52–$33.46 Per Hour

The Research Assistant will be responsible for conducting literature searches, data management, recruiting participants, obtaining consents, maintaining files, scheduling and conducting interviews of patients and family members, maintaining data collection files, assisting with data analysis and generating correspondence, reports and graphics. Analytical ability is required to prepare reports, maintain data inventory, code, transcribe interviews, develop graphs, perform literature searches, negotiate systems in several hospitals and/or human service organizations, and identify concerns/responses of participants that require termination of interview or possible intervention.

Chicago, IL30+ days ago

$19.89–$27.97 Per Hour

Completes all activities by strictly following Good Clinical Practices (GCP) & all relevant current local, state, & federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board (IRB), Food & Drug Administration (FDA) Code of Federal Regulations (CFR), & the International Conference on Harmonization (ICH). Job Summary: Coordinates collection, analysis, processing & reporting of data & assists Principal Investigator (PI) in judging the validity of test data obtained in regard to biomedical &/or social-behavioral research study(ies) of limited complexity involving co-investigators, multiple campuses &/or universities.

New!

Trout Valley, IL3 days ago

$40–$42 Per Hour
Temporary

Required Education: Bachelor's degree in chemistry Required Experience/Skills: 6+ years of hands-on experience with analytical instrumentation, including HPLC, GC, FTIR, UV-Vis, and related laboratory equipment. Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify).

Downers Grove, IL30+ days ago

$24.36 Per Hour
Part-time

More than 6,000 full-time students are enrolled in graduate programs in osteopathic medicine, dentistry, pharmacy, physician assistant studies, physical therapy, occupational therapy, nurse anesthesia, cardiovascular perfusion, podiatry, optometry, clinical psychology, speech language pathology, biomedical sciences and veterinary medicine. The Research Assistant is expected to assist in the training of students, design and execution of research experiments, collection and analysis of data, generation of figures and presentations for the collected data, and revising manuscripts that involve these data.

Chicago, IL30+ days ago

$24.04–$28.85 Per Hour

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. The Clinical Research Technician works closely with Scientific Directors and Research Managers to support research design, regulatory compliance, participant engagement, and data analysis, contributing to the preparation of reports, publications, and presentations.

New!

Chicago, IL6 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

New!

Chicago, IL6 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.

Round Lake, IL22 days ago

$26–$28 Per Hour

Since our formation in 2002, organizations across commercial and public sectors have been trusting us to help build their teams with exceptional temporary and permanent talent. DivIHN, the 'IT Asset Performance Services' organization, provides Professional Consulting, Custom Projects, and Professional Resource Augmentation services to clients in the Mid-West and beyond.

Chicago, IL30+ days ago

Remote

$95,000–$130,000 Per Year

As a senior member of Huron's Research Office team, you will negotiate and prepare clinical research study contracts that include Confidentiality Agreements, Non-Disclosure Agreements, Clinical Trial Agreements, Nonconforming Subcontracts, Master Service Agreements, Material Transfer Agreements, and Data Transfer Agreements. You'll help our clients to achieve organizational effectiveness, improve student outcomes, implement new technologies and align resources and investments to ensure long-term sustainability.

Peoria, Illinois30+ days ago

$42.64–$56.50 Per Hour

As Manager, HSPP, you will lead and evolve OSF’s Human Research Protection Program within a single FWA environment, supporting a diverse portfolio of clinical, academic, and investigator-initiated research -- largely in reliance with external IRB -- while maintaining strong institutional oversight and accountability. Familiarity with Epic and research functionality, Experience conducting human subjects research, Post approval monitoring, project management, policy development, research ethics, experience in industry clinical trial space, experience working with academic/university partners, research-related contracts (e.g.

Chicago, IL30+ days ago

$19.89–$24.86 Per Hour

Primary responsibilities may include scheduling research participants, administering neuropsychological tests, coordinating with interdisciplinary teams within the Institute, transcribing speech samples, processing participant payments, data entry/maintenance of a REDCap database, processing of neuroimaging, preparing data for faculty/investigators and grant-related reports, and working on study-related research projects. Minimum Qualifications: Successful completion of a full 4-year course of study in an accredited college or university leading to a bachelors or higher degree in a major such as social or health science or related; OR appropriate combination of education and experience and 2 years research study or other relevant experience required; OR.

Chicago, IL30+ days ago

$38.46–$52.88 Per Hour

Our state-of-the-art Comer Childrens Hospital allows our faculty to enhance and expand their innovative and pioneering work in hybrid surgery: a minimally invasive, off-pump approach for newborns suffering from hypoplastic left heart syndrome. We were the first to perform a DaVinci-assisted coronary artery bypass graft surgery in Chicago and routinely perform minimally invasive valve surgeries, including complex redo valves.

Peoria, Illinois17 days ago

$33.52–$45.49 Per Hour

Ability to thrive in both a heads-down, independent work environment as well as work on team projects collaboratively -Proficiency with identifying, interpreting, and applying the multiple regulatory frameworks governing conduct of research (e.g., Office for Human Research Protections (OHRP), Food and Drug Administration (FDA), Health Insurance Portability and Accountability Act (HIPAA), National Institutes of Health (NIH). The RCA acts as a liaison between research teams, the institution(s), and the Institutional Review Boards (IRBs), safeguarding the interests of all parties & participants involved in the conduct and oversight of human subject research.

Chicago, IL30+ days ago

$51,346–$72,532 Per Year

Ability to manage and maintain accurate clinical research documentation and data Familiarity with medical terminology and basic concepts in healthcare and clinical research Strong verbal and written communication skills for interacting with study participants, investigators, and other stakeholders Basic proficiency with Microsoft Office Suite (Word, Excel, Powerpoint) Ability to clearly explain study procedures and obtain informed consent from participants Ability to manage multiple tasks and prioritize effectively Strong attention to detail and accuracy in data collection and documentation Ability to work collaboratively in a team environment Professionalism and ethical conduct in handling sensitive information and interacting with study participants Sensitivity to the needs and concerns of study participants Commitment to ensuring participant safety and well-being throughout the study. Minimum Qualifications: (Education, experience, and any other certifications or clearances) Successful completion of a full 4-year course of study in an accredited college or university leading to a bachelors or higher degree in a major such as social or health science or related; OR appropriate combination of education and experience and 2 years research study or other relevant experience required; OR Successful completion of a full course of study in an accredited college or university leading to a masters or higher degree in a major such as social or health science or related; OR appropriate combination of education and experience and 1 year research study or other relevant experience.

Chicago, IL30+ days ago

$24.04–$33.65 Per Hour

Specifically, the Research Analyst will be investigating the role of and therapeutic targets of the stroma during ovarian cancer disease progression, and will involve human tissue, in vivo mouse models, three-dimensional organotypic, and primary cell models to perform translational research. Maintains recruiting and scheduling research subjects; assisting with developing or amending study protocols; assisting with developing data collection tools; assisting with building databases; and providing general administrative support.

Hyde Park, IL30+ days ago

$65,000–$90,000 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, IL30+ days ago

$50,000–$65,000 Per Year

The Pediatric Clinical Trials Office (Peds CTO) is an existing centralized support office that provides services and high-level guidance to individuals (faculty, investigators, research staff, and clinic coordinators from the University and Hospital) involved in human subjects research. The CRC 1 will be involved in multiple research trial types: multi-centered cooperative group and intergroup studies at a national level, multi-institutional pharmaceutical trials, and multi-centered trials designed, implemented and coordinated in the Section.

New!

Hyde Park, IL6 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

$17.05–$21.31 Per Hour

Minimum Qualifications: Successful completion of a full 4-year course of study in an accredited college or university leading to a bachelors or higher degree in a major such as social or health science or related; OR appropriate combination of education and experience. This person will obtain consent, ensure blood samples are obtained, enter and analyze data, and participate in the writing of peer-reviewed manuscripts and additional grant applications.

New!

Chicago, IL6 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. Maintains accurate and complete records which may include, but are not limited to, signed informed consent, relevant IRB approvals, source documentation, Case Report Forms (CRF's), drug dispensing logs, and study related communication.

Hyde Park, IL30+ days ago

$70,000–$95,000 Per Year

The Payments and Research Revenue Specialist is an integral part of the Office of Clinical Research, responsible for overseeing the accurate processing and allocation of clinical research revenue, including remittances from grants and clinical trial payments in the Electronic Medical Record (Epic EMR). The position supports continuous improvement initiatives, monitors and resolves outstanding items in EMR work queues for clinical research accounts, and ensures adherence to institutional, federal, and sponsor policies governing clinical research payment processing and revenue documentation.

Chicago, IL30+ days ago

Various voluntary benefits: • Supplemental Life, AD&D and Disability • Critical Illness, Accident and Hospital Indemnity coverage • Tuition assistance • Student loan servicing and support • Adoption benefits • Backup Childcare and Eldercare • Employee Assistance Program, and other specialized behavioral health services and resources for employees and family members • Discount on services at Lurie Childrens facilities • Discount purchasing program. 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.

Elgin, IL30+ days ago

Full-time

Additional Qualifications: Database and computer skills: Microsoft Office (Word, Excel), Outlook, excellent verbal and written communication skills, ability to work independently and assume responsibility, excellent organizational skills, ability to meet data deadlines and maintain confidentiality. Education/ Training: International Medical Graduate; MBBS, BMBS, MBChC, MBBCh, MD, DO, MCM, DM, MCM, MMSc, MMedSc, MM, MMed, MS, MSurg, MChir, MCh, ChM, CM, MSc, DCM, DClinSurg, DMSc, DMedSc, DS, DSurg.

Chicago, IL30+ days ago

Maintains recruiting and scheduling research subjects; assists with developing or amending study protocols; assists with developing data collection tools; assists with building databases; and provides general administrative support. • Analyzes study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.

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Winter Research Jobs in Illinois

Assistant/Associate/Professor of Clinical Pediatrics Physical Medicine and Rehabilitation Physician University of Illinois College of Medicine Peoria

Corporate Transfer Pricing Intern - Winter 2027 Illinois Tool Works Inc

Winter/Spring 2027 Consulting Services Intern - Gaming RubinBrown LLP

Winter/Spring 2027 Consulting Services Intern - Risk Services RubinBrown LLP

Clinical Research Assistant, PRN (Registered Nurse) Care Access

Clinical Research Assistant, PRN Care Access

Research Coordinator-Hernia Research Endeavor Health

Clinical Research Associate Zp Group Llc

Clinical Research Nurse 1 - Cancer Research Rush University Medical Center

Clinical Research Assistant University Retina

Director Clinical Research Operations OSF HealthCare

Manager Clinical Research Monitoring OSF HealthCare

Senior Clinical Research Associate ICON Plc

RN - Manager Clinical Research Gables Search Group

Clinical Research Assistant Illinois Institute of Technology

Clinical Research Monitor OSF HealthCare

Manager Clinical Research Oncology OSF HealthCare

Associate Professor, Clinical Imaging Research - CFH Carle Health

Clinical Research Coordinator Genesis Orthopedics & Sports Medicine

Clinical Research Coordinator I Ora Inc

Director Research Operations & Standardization OSF HealthCare

Research Assistant- IL- Pharmacy Practice Midwestern University

Clinical Research Assistant Rush University Medical Center

Clinical Research Assistant - Orthopedic Surgery Rush University Medical Center

Clinical and Health - Clinical Research Coord II Mindlance

Clinical Research Coordinator I University of Chicago

Research Assistant - CBM Shirley Ryan AbilityLab

Research Study Coordinator, Pulmonary Northwestern University

Research & Development Clinical Scientist Jobs in USA, IL, Cary | Rose International Job Rose International

Research Assistant- IL- Biochemistry & Molecular Genetics Midwestern University

Clinical Research Technician, MOSAAIC Study of Asian Americans University of Chicago

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

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

Research Associate Scientific I DivIHN Integration Inc

Sr Research Contract Specialist- US-REMOTE Huron Consulting Group Inc

Manager Clinical Research Human Subject Protection Program OSF HealthCare

Research Study Coordinator Northwestern University

Research Lab Manager University of Chicago

Research Compliance Analyst OSF HealthCare

Clinical Research Coordinator Northwestern University

Research Assistant University of Chicago

Regulatory Affairs Manager, Research Incubation Unit University of Chicago

Clinical Research Coordinator 1 - Pediatrics University of Chicago

Clinical Research Coordinator 2, Department of Surgery University of Chicago

Research Study Assistant Northwestern University

Clinical Research Coordinator II University of Chicago

Payments and Research Revenue Specialist University of Chicago

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

International Medical Graduate (IMG) - Clinical Research Coordinator Revival Research Institute, LLC

Research Analyst University of Chicago

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