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
- ...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
$60k - $75k
...Clinical Research Coordinator II The Clinical Research Coordinator II (CRC II) is an onsite, patient... ...startup through closeout including recruitment and screening of study subjects, obtaining informed consent, collecting research data, and ensuring protocol adherence...DataWork experience placement- ...Clinical Research CoordinatorAt DOCS Dermatology Group, we are not just one of the... ...detail-oriented Clinical Research Coordinator to join our growing team. The ideal... ...studies, including participant recruitment, informed consent, and data collection.Collaborate with principal...DataContract work
- ...Health Systems Clinical Research Job Title: Clinical Research Coordinator I Department: Clinical Research... ..., including participant recruitment, screening, enrollment, and data collection. This role... ...Obtain and document informed consent in compliance with ICH-...DataFull timeMonday to Friday
- ...Clinical Research Coordinator I The MICU Research Program, with Dr. Krysta Wolfe... ...maintenance of datasets and data collection for a variety of... ...documentation of signed informed consent, relevant IRB approvals,... ...study meetings. May recruit and interview potential study...DataWork experience placement
$23.12 - $32.66 per hour
...industry specific market data. The pay range for each role... ...of each case. The Clinical Research Coordinator I supports neurology movement... ...Responsibilities include participant recruitment and interaction, study... ...: 1. Recruits, consents, screens, schedules, tracks...DataHourly payFull timeLocal areaShift workNight shiftWeekend workAfternoon shift$31 per hour
...Clinical Research Coordinator IIThe Clinical Research Coordinator II is responsible for the... ...complete annual protocol renewals. Recruit, screen, assist in the informed consent process and enroll subjects in... ..., record and maintain complete data files using good clinical...DataHourly payWork experience placementLocal area- ...Clinical Research Coordinator The Clinical Research Coordinator manages and directs... ...effective patient recruitment strategies, research budgets... ...Research, clinical trials, data & protocol management Lead... .... Execute informed consent process and monitors patient...DataWork at office
$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$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- ...Clinical Research CoordinatorEnvisioning and implementing a holistic... ...The Clinical Research Coordinator (CRC) will work... ...protocols and informed consents, and ensure eligibility criteria and recruitment.Coordinate all study visits... ...adverse events to the Data Safety and Monitoring...DataInterim roleLocal area
$50k - $65k
...Department BSD OCR - Clinical Research Operations About... ...Clinical Research Coordinator I- Office of Clinical... ...enrollment, study visits, data collection, and... ...documentation of signed informed consent, relevant IRB... ...groups. May recruit and screen potential...DataFull timeWork experience placementWork at office- ...Clinical Research Coordinator I - Oral Health Research StaffThe position is a Clinical... ...screening and informed consent for potential study enrollees... ...enrollees.Protects patients and data confidentiality by ensuring... ..., or progress reports.Recruit participants for other clinical...DataWork experience placementWeekend workAfternoon shift
$49.92k - $81.62k
...medical technology, research and family-friendly design... ...of Chicago Coordinates all clinical research activities with... ...and administrative data tasks varies according... ...conducting informed consent processes, coordinating... ..., consult your recruiter or click the following...DataHourly payFull timePart timeFlexible hours$51.35k - $64.47k
...Department: MED-Clinical Trials Unit Salary/... ...alignment with market data. Job Summary:... .../or social-behavioral research study involving multidisciplinary... ...& publication & coordinates writing, submission &... ...sponsors; completes informed consent; determines &...DataWork at officeLocal area$59.28k - $96.93k
...medical technology, research and family-friendly design... ...211 E Chicago Coordinates all clinical research activities... ..., patient facing vs. data administrative responsibilities... ...by identifying and recruiting eligible subjects, conducting informed consent/assent processes,...DataHourly payFull timePart timeFlexible hours- 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
- The University of Chicago seeks a Clinical Research Coordinator 2 (CRC2) to partner with the Principal Investigator and a research manager to... ...Responsibilities include screening, enrollment, scheduling, informed consent, data collection, and ensuring protocol adherence, with focus...Data
- 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
- ...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
- 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
- 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
- ...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
- ...Clinical Research Coordinator The Breathe Chicago Center (BCC) in the Department of Medicine... ...managers, as well as lab, data, and admin staff. Clinical... ...implementation and management, participant recruitment and retention, executing informed consent, and compliance with...DataWork at office
$60k - $75k
Clinical Research Coordinator II BSD MED - Endocrinology - Pannain Research Staff Job... .... Responsibilities Recruit, screen, and enroll eligible... ...participants. Obtain informed consent and provide detailed study... ...patient status, collect clinical data, and report adverse events....DataWork experience placement$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$49.92k - $81.62k
Coordinates all clinical research activities with moderate supervision. Adheres to the service values and principles... ...patient‑facing and administrative data tasks varies according to the... ...eligible subjects, conducting informed consent processes, coordinating reimbursement...DataFlexible hours$50k - $75k
Clinical Research Coordinator - University of Illinois Chicago, Chicago, IL, USA... ...treatment schedules, develops recruitment strategies, and... ...scheduling, testing, and data management for multi‑faceted... ...phlebotomy. Execute informed consent process and monitor patient...DataWork at office$49.92k - $81.62k
Essential Job Functions Coordinates and manages the initiation and regulatory compliance of clinical research studies, including preparing all... ...proper processing, records data on source documents and electronic... ..., conducting informed consent processes, coordinating reimbursement...DataHourly payFull timePart timeFlexible hours$60k - $75k
## Clinical Research Coordinator II, SurgeryApplyremote type: Onsitelocations: Chicago... ...institutional pharmaceutical.* Recruits and screens study subjects, obtains informed consent, enrolls subject in research... ...and analyzes research data, completes the case report form...DataWork experience placement
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