Clinical Research Coordinator: Data, Recruitment & Consent
$21.5 - $24.85 per hourNorthwestern University
Target hiring range for this position will be between $21.50-$24.85 per hour. Offered salary will be determined by the applicant's education, experience, knowledge, skills and abilities, as well as internal equity and alignment with market data. 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. 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). Specific Responsibilities : Technical Participates in the planning & conduct of research study including participant recruitment and retention. Obtains informed consent Collects, compiles, tabulates & processes responses. Gathers information. Extracts & analyzes data from medical charts. Completes basic clinical procedures such as drawing blood & obtaining blood pressure. Administration Collates relevant mathematical results & prepares tables, charts & graphs reflecting relationships of multiple tests. Prepares reports for investigators and sponsors on recruitment status and other pertinent study data. Writes portions of grant applications & co-author scientific papers. Completes documents associated with current local, state, & federal regulatory guidelines, requirements, laws & research protocols. Finance May process payments for research participants per study protocol. Works with industry representatives to negotiate tentative grant funding. Coordinates reimbursements for expert panel travel, consultant pay, additional gift card orders, etc. & ensure costs remain within allotted grant budget. Supervision May provide work direction &/or train other research staff to interview/test participants. May act as a mentor in regard to education of junior coordinators. Performs other duties as assigned. 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 bachelor's 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 master's or higher degree in a major such as social or health science or related; OR appropriate combination of education and experience. Must complete NU's IRB CITI training before interacting with any participants & must re-certify every 3 years. Benefits: At Northwestern, we are proud to provide meaningful, competitive, high-quality health care plans, retirement benefits, tuition discounts and more! Visit us at to learn more. Work-Life and Wellness: Northwestern offers comprehensive programs and services to help you and your family navigate life's challenges and opportunities, and adopt and maintain healthy lifestyles. We support flexible work arrangements where possible and programs to help you locate and pay for quality, affordable childcare and senior/adult care. Visit us at to learn more. Professional Growth & Development: Northwestern supports employee career development in all circumstances whether your workspace is on campus or at home. If you're interested in developing your professional potential or continuing your formal education, we offer a variety of tools and resources. Visit us at to learn more . Northwestern University is an Equal Opportunity Employer and does not discriminate on the basis of protected characteristics, including disability and veteran status. View Northwestern's non-discrimination statement . Job applicants who wish to request an accommodation in the application or hiring process should contact the Office of Civil Rights and Title IX Compliance. View additional information on the accommodations process . #J-18808-Ljbffr Northwestern University
$22.25 - $36.38 per hour
...medical technology, research and family-friendly... ...implementation, coordination, and conduct of clinical research activities... ...and administrative data tasks varies according... ..., informed consents, modifications, renewals... ...identification and recruitment of eligible study subjects...DataHourly payFull timePart time- ...of Chicago is seeking a Clinical Research Assistant to support investigators in coordinating and conducting pediatric... ...patient-facing tasks with data management and regulatory... ...regulatory binders, informed consents, and IRB submissions; help recruit eligible subjects; and...Data
- ...Our client is seeking a Clinical Research Coordinator to lead the execution of complex clinical trials... ...a resource on assigned projects Recruit, screen, and consent study participants in compliance... ...protocol Accurately document and enter data into EDC and resolve queries per...DataPrivate practice
- ...Clinical Research Coordinator IThe Section of Pulmonary/Critical Care has been a model... ...of datasets and data collection for a variety of... ...documentation of signed informed consent, relevant IRB approvals, source... ...study meetings.May recruit and interview potential study...DataWork experience placement
$49.92k - $81.62k
...Pediatric Clinical Research CoordinatorAnn & Robert H. Lurie... ...facing and administrative data tasks varies... ...Essential Job Functions:Coordinates and manages the initiation... ...conducting informed consent processes,... ...compensation, consult your recruiter or click the following...DataHourly payFull timePart time- ...Clinical Research Coordinator Envisioning and implementing a holistic approach to neurological... ...protocols and informed consents, and ensure eligibility criteria and recruitment. Coordinate all study... ...Report adverse events to the Data Safety and Monitoring Board,...DataTemporary workInterim roleLocal area
$29.36 - $42.61 per hour
...Department: Pediatric Neurology Research Work Type: Full Time... ...industry specific market data. The pay range for each... ...: Job Summary: The Clinical Research Regulatory Coordinator 2 (CRRC 2) prepares,... ...submit IRB materials such as consent forms, new study...DataHourly payFull timeContract workWork at officeShift work$31 per hour
...Position Details Job Title CLINICAL RESEARCH COORDINATOR II Position Number 815002... ...annual protocol renewals. Recruit, screen, assist in the informed consent process and enroll subjects in... ..., record and maintain complete data files using good clinical practice...DataHourly payFull timeWork experience placementLocal area$60k - $77k
...Senior Clinical Research Coordinator Senior Clinical Research... ...such as available market data, internal equity, candidate... ...implements effective patient recruitment strategies, research budgets... ...projects. Execute informed consent process and monitors patient...DataWork at officeWorldwide$51.35k - $64.47k
...this Job Department: MED-Clinical Trials Unit Salary/... .../or social-behavioral research study involving multidisciplinary... ...& publication & coordinates writing, submission &... ...; completes informed consent; determines &... ...& treatment schedule. Data Manages project data including...DataWork at officeLocal areaFlexible hours$29 - $31.5 per hour
...Job Title: Clinical Research CoordinatorJob Description The Clinical Research Coordinator plays a central role in the... ...participant safety and data quality.... ...+ Lead participant recruitment and screening activities... ...including informed consent forms and other essential...DataContract workTemporary work$65k - $80k
...commitment to excellence in clinical care, education, and research. Its faculty bring... ...Summary The Clinical Research Coordinator III coordinates and... ...participant activities, data collection, REDCap administration... ..., including the informed consent process, study activities...DataWork experience placementWork at office- The University of Chicago is seeking a Clinical Research Coordinator II for Gastroenterology to manage all... ...with subjects, and ensure accurate data entry and adverse event reporting under... ...through closeout, obtaining informed consent, scheduling procedures, and educating...Data
- The Clinical Research Coordinator II (CRCII) at The University Of Chicago partners with the Principal Investigator in the Endocrinology section to recruit, consent, and monitor study participants, collect data and specimens, and ensure adherence to GCP and all regulatory...Data
- University of Chicago is seeking a Clinical Research Coordinator II to partner with the PI in endocrinology research. You will recruit and enroll participants, obtain consent, and monitor patient status while ensuring data integrity and regulatory compliance. The role requires...Data
- The University of Chicago in Chicago, IL seeks an onsite Clinical Research Coordinator II to support neurology clinical trials under the... ...the Clinical Research Manager. You will handle screening, consent, data collection, adverse event reporting, and coordination of...Data
- ...University in Chicago is seeking a Research Study Coordinator to support biomedical and behavioral research. You will coordinate data collection, processing, and reporting... ...Responsibilities include participant recruitment and consent, administering tests, extracting...Data
- ...motivated, organized, and detail-oriented Clinical Research Coordinator to join our growing research... ...active studies simultaneously • Recruit, screen, consent, and schedule study participants... ...accurate source documentation and timely data entry • Enter and maintain study...DataFull timeMonday to Friday
- ...Sciences Division at the University of Chicago seeks a Clinical Research Coordinator II to support daily trial activities onsite, partnering... ...Manager. The CRC II coordinates screening, enrollment, consent, data collection, and adverse event reporting in line with protocol...Data
- ...Division, Endocrinology Section, seeks a Clinical Research Coordinator II to work with the PI Dr. Silvana... ...coordinate participant enrollment, data collection, and study logistics within... ...Responsibilities include obtaining informed consent, ensuring GCP compliance,...Data
- ...Chicago's BSD MED - Hematology and Oncology is seeking a Clinical Research Coordinator 2 (CRC2) to partner with the PI and manage daily... .... Responsibilities include screening, enrollment, data collection, informed consent, adverse event reporting, site visits, and ensuring...Data
- Rush University Medical Center in Chicago is seeking a Clinical Research Coordinator I to support a range of clinical studies. You will recruit and consent participants, collect data, maintain regulatory documents, and communicate with sponsors under supervision. Requirements...Data
- The University of Chicago is seeking a Clinical Research Coordinator I for the BSD Hematology/Oncology - Clinical Research Staff, Cluster 9.... ...national and intergroup levels, coordinating protocols, consents, and data collection. Education includes a college degree in a...Data
- ...Health Systems Clinical Research Job Title: Clinical Research Coordinator I Location: On-site (Insight Hospital... ..., including participant recruitment, screening, enrollment, and data collection. This role... ...Obtain and document informed consent in compliance with ICH-...DataFull timeMonday to Friday
$60k - $75k
...Clinical Research Coordinator II The Clinical Research Coordinator II (CRCII) is a specialized... ..., and adverse event reports. Recruits and interviews potential study... ...subjects, obtaining informed consent, collecting research data, and ensuring protocol adherence...DataWork experience placementWork at office- Rush University Medical Center in Chicago, IL, is seeking a Clinical Research Coordinator I to support multiple studies under supervision. You will recruit, screen, consent, and schedule participants; collect data; maintain regulatory documents; and communicate with...Data
$30 - $38 per hour
Senior Clinical Research Coordinator - Permanent - Chicago, IL Are you ready to make a groundbreaking... ...-oriented with a commitment to data accuracy, patient safety, and regulatory... ...providing guidance and training. Recruit, screen, and consent study participants in accordance...DataHourly payPermanent employmentPrivate practice$60k - $72k
Clinical Research Coordinator in Chicago, IL (60640) Overview: We are seeking a detail-oriented Clinical... ...highest standards of compliance, data quality, and patient care. The... ...including participant recruitment, informed consent, visit scheduling, and protocol compliance...DataMonday to Friday$29.36 - $42.61 per hour
...Center Department: ER Research Recruit - Gottlieb Work Type:... ...industry specific market data. The pay range for each role... ...at Rush is looking for a Clinical Research Coordinator III that values a fast-paced... ...study including recruitment, consent, screening, scheduling,...DataHourly payFull timeLocal areaShift work$60k - $78k
...all the relevant clinical trial documentation. Completing data entry and query resolution... ...Investigators, Research Participants and... ...knowledge of the recruitment and retention... ...Protocols, Informed consents, Study Manuals, and... ...preferably with practice coordinating industry-sponsored...Data
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