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
$27.47 - $38.81 per hour
...industry specific market data. The pay range for each role... .... Job Summary: The Clinical Research Coordinator II (CRC II) independently... ...Responsibilities include participant recruitment and retention, study data... ...including recruitment, consent, screening, scheduling,...DataHourly payFull timeLocal areaShift workWeekend workAfternoon shift- ...Clinical Research Coordinator 2 The Clinical Research Coordinator 2 (CRC2) is a... ...include, but are not limited to, recruitment and screening of study subjects, obtaining informed consent, enrollment of subject in... ...and analyzing research data, completion of the case report...DataWork experience placement
$23.12 - $32.66 per hour
...industry specific market data. The pay range for each role... .... Job Summary: The Clinical Research Coordinator I (CRC I) supports the conduct... ...include participant recruitment and interaction, study data... ...Responsibilities: # Recruits, consents, screens, schedules,...DataHourly payFull timeLocal areaShift workNight shiftWeekend workAfternoon shift$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$60k - $75k
...Clinical Research Coordinator II The Section of Hematology/Oncology has a proud and long tradition... ..., and adverse event reports. Recruits and interviews potential study... ...subjects, obtaining informed consent, collecting research data, and ensuring protocol adherence...DataContract workWork experience placementWork at office$49.92k - $81.62k
...medical technology, research and family-friendly design... ...Job Description Coordinates all clinical research activities... ...and administrative data tasks varies according... ...conducting informed consent processes, coordinating... ..., consult your recruiter or click the following...DataHourly payFull timePart timeFlexible hours$50k - $70k
...Clinical Research Coordinator Clinical Research Coordinator Hiring Department... ...effective patient recruitment strategies, and participating... ...scheduling, testing, and data management for a multi-faceted... ...~ Execute informed consent process and monitor patient...DataWork at officeWorldwide$50k - $65k
...Department BSD DFI - Clinical Studies About... ..., physicians, data analysts, and... ...impact clinical research conducted across... ...clinical research coordinator will assist in all... ...-person patient consent. Transport patient... ...participant recruitment, and patient consent...DataWork experience placementShift work$51.35k - $72.53k
...alignment with market data. Job Summary: Manages... .../or social-behavioral research study involving... ...presentation & publication & coordinates writing, submission &... ...following Good Clinical Practices (GCP) & all... ...sponsors; completes informed consent; determines &...DataWork at officeLocal areaFlexible hours$46.28k - $75.67k
...Pediatric Clinical Research Coordinator Ann & Robert H. Lurie Children's Hospital of Chicago... ...and IRB support, participant recruitment and coordination, REDCap-based data collection and management,... ...preparation of protocols, informed consents, modifications, renewals and...DataHourly payFull timePart timeFlexible hours- Actalent is seeking a Clinical Research Coordinator for a contract position in Hinsdale, IL. The coordinator will manage multiple study... ...in conducting screenings, obtaining informed consent, and managing study data accurately. This role is designed for someone committed...DataContract work
$31 per hour
...Clinical Research Coordinator II The Clinical Research Coordinator II is responsible for... ...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$50k - $65k
...Clinical Research Coordinator I The Section of Pulmonary/Critical Care has been... ...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$25 - $40 per hour
...Clinical Research Coordinator (Contract Position) Contract Duration: Open-ended... ...Responsibilities Participant Recruitment & Screening Identify,... ...Obtain informed consent from participants in accordance... ...information as needed. Data & Documentation Management...DataContract workTemporary workFor contractorsImmediate start- ...Senior Clinical Research Coordinator The Center for Clinical and Translational... ...implements effective patient recruitment strategies. Oversees all... ...and procedures. Extract data from complex medical... ...phlebotomy. Execute informed consent process and monitor...DataWork at office
- ...Visiting Senior Clinical Research Coordinator The Breathe Chicago Center (BCC) in... ...managers, lab technicians, and data staff; and communicates... ...Coordinators are responsible for recruiting and retaining participants;... ...plans. Informed Consent and Regulatory Requirements...DataShift work
- ...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
- Position: Clinical Research Coordinator III Location: Chicago, IL Job Id: 1152... ...provide the best quality data to the sponsor. To ensure... ...working knowledge of the recruitment and retention process for... ...Study Protocols, Informed consents, Study Manuals, and all the...Data
- ...Department BSD SUR - Research Services:... ...influence standard clinical practice. Today, the... ...Clinical Research Coordinator 2 (CRC2) is a specialized... ...pharmaceutical studies. Recruitment and screening of... ...obtaining informed consent, enrollment, follow-up, data collection and analysis...DataWork experience placement
$49.92k - $81.62k
Job Summary Coordinates all clinical research activities with moderate supervision. Adheres to the service values... ...patient-facing and administrative data tasks varies according to the... ...eligible subjects, conducting informed consent processes, coordinating reimbursement...DataFlexible hours$25 per hour
Position Overview Clinical Research Coordinator (Contract Position). This contractor... ...Participant Recruitment & Screening Identify, recruit... ...Conduct Obtain informed consent from participants in accordance... ...and information as needed. Data & Documentation Management...DataContract workTemporary workFor contractorsMonday to Friday$46.28k - $75.67k
...pediatric care and is seeking a Clinical Research Coordinator to assist investigators and... ...protocols, informed consents, modifications, renewals, and... ...projects and identify and recruit eligible study subjects. Maintain... ...templates. Abstract data from medical records and enter...DataFlexible hours$46.28k - $75.67k
The Clinical Research Coordinator (CRC) will focus on the Glycemia Range and Offspring... ...protocols, informed consents, modifications, renewals, and... ...implementing projects and identify/recruit eligible study subjects.... ...templates. Abstract data from medical records and enter...DataFlexible hours$29.36 - $42.61 per hour
...Medical 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-... ...study including recruitment, consent, screening, scheduling,...DataHourly payFull timeLocal areaShift work- ...goal, and our unique research and powerful solutions... ..., human touch. The Clinical Research Coordinator (CRC) will work collaboratively... ...and informed consents, and ensure eligibility criteria and recruitment. Coordinate all... ...adverse events to the Data Safety and Monitoring...DataTemporary workInterim roleLocal area
$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$59.28k - $96.93k
General Summary Coordinates all clinical research activities with minimal supervision. Adheres... ..., patient‑facing versus data‑administrative responsibilities... ...studies by identifying and recruiting eligible subjects, conducting informed consent/assent processes,...DataFull timePart timeFlexible hours$50k - $65k
...Department The Office of Clinical Research (OCR) was created to... ...Clinical Research Coordinator I (CRC I) supports routine... ..., study visits, data collection, regulatory... ...of signed consents, IRB approvals, source... ...assurance audits, and may recruit and screen study participants...DataWork experience placementWork at office- Position Title Clinical Research Coordinator I Department Global Project Delivery... ...-site study visit support, data collection, protocol compliance... ...tasks such as informed consent, medical history documentation... ...investigators. Screen, recruit, and enroll patients and perform...DataDaily paidFull timeContract workFlexible hoursWeekend work
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