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
$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 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
$50k - $65k
...Medicine - Beiser Research Staff About the... ...administrative and clinical personnel who are devoted... ...Clinical Research Coordinator 1 (CRC1) is a... ...closeout including recruitment and screening of study... ...obtaining informed consent, collecting research data, and ensuring protocol...DataFull timePart timeWork experience placement- ...Clinical Research Coordinator Location: Chicago, IL Experience: Entry-Level... ...research operations, and data management . The ideal... ...study start-up, participant recruitment, enrollment, scheduling,... .... Assist with informed consent processes in accordance with...DataFull timeInternshipCurrently hiringWork at office
$59.28k - $96.93k
...medical technology, research and family-friendly design... ...Job Description Coordinates all clinical research activities... ..., patient facing vs. data administrative... ...studies by identifying and recruiting eligible subjects, conducting informed consent/assent processes,...DataHourly payFull timePart timeFlexible hours$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: 1. Recruits, consents, screens, schedules,...DataHourly payFull timeLocal areaShift workNight shiftWeekend workAfternoon shift- The University of Chicago seeks a Clinical Research Coordinator 1 in Rheumatology to support the PI and... ...Reid Research Staff. You will manage consent, approvals, and documentation, coordinate... ...communication, organization, and data-management skills. Onsite work in Chicago...Data
$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- 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
- ...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
- 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
$46.28k - $75.67k
...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 timeFlexible hours$70k - $90k
...Visiting Senior Clinical Research Coordinator - Department of Medicine, Breathe Chicago... ..., lab technicians, and data staff; and communicates with... ...Coordinators are responsible for recruiting and retaining participants;... ...plans. Informed Consent and Regulatory Requirements...DataFull timeWorldwideShift work$50k - $65k
...Clinical Research Coordinator I - Oral Health Research Staff The position is a Clinical... ...screening and informed consent for potential study... .... Protects patients and data confidentiality by ensuring... ...documents, or progress reports. Recruit participants for other...DataWork experience placementWeekend workAfternoon shift$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 - $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- ...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
$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- ...are seeking a highly motivated and detail-oriented Clinical Research Coordinator to join our growing team. The ideal candidate will... ...clinical research studies, including participant recruitment, informed consent, and data collection. Collaborate with principal investigators...DataContract work
$50k - $65k
...Medicine - Del Rios Research Staff About The Department... .... Job Summary The Clinical Research Coordinator 1 will be... ...based, clinical, and data-driven projects; managing... ...with participant recruitment and enrollment; organizing... ...including informed consent, participant...DataWork experience placement- ...Clinical Research Coordinator Assistant Envisioning and implementing a holistic... ...including the production of a recruitment tool, and progress notes,... ...notes, and collects study data via source documents/... ...as conducting the informed consent process Assists other staff...DataTemporary workLocal areaImmediate start
$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- ...Sciences - Oral Health Research Staff About the... ..., brainstorms and coordinates new research... ...Medicine on multiple clinical research studies.... ...screening and informed consent, administers... ...Protects patient and data confidentiality by... ...reports. Recruits participants for other...DataWeekend workAfternoon shift
- ...to highlight our exciting Clinical Research Associate opportunites! We... ...qualified Clinical Research Coordinators and Research Nurses to attend... ...against case report form data, including informing the site... ...research site’s patient recruitment and retention success and offering...DataContract workWork at officeRemote workWork from homeHome officeFlexible hours
- ...Anesthesiology Research Study Manager Manages daily operations... ...presentation & publication & coordinate writing, submission & administration... ...by strictly following Good Clinical Practices (GCP) & all current... ...activities per protocol. Data: Manages project data...DataLocal area
$28 per hour
...Position Details Position Details Job Title CLINICAL RESEARCH COORDINATOR I Position Number 8151017 Work Modality Hybrid -... ...processing. Collect and manage patient and laboratory data for clinical research projects. Manage research project databases...DataHourly payFull timeWork experience placementWork at officeLocal area$50k - $75k
The University of Illinois - Chicago is seeking a Clinical Research Coordinator to manage clinical research protocols within the Center for Clinical and Translational Science. Responsibilities include implementing and conducting research projects, ensuring compliance with...- The University of Chicago in Chicago, IL seeks a Clinical Research Coordinator II to partner with the PI and Clinical Research Manager in the Gastroenterology... ..., ensuring protocol adherence, and safeguarding patient data and regulatory compliance. Responsibilities include...Data
- Rush University Medical Center is seeking a Clinical Research Coordinator I to support clinical studies. Responsibilities include recruiting participants, collecting data, and ensuring compliance with research protocols. The ideal candidate will have strong problem-solving...DataFull time
- ...Children’s Hospital of Chicago is seeking a Clinical Research Support role to assist investigators... ...protocol preparation, and participant coordination. The position emphasizes adherence to FDA/HSR/GCP guidelines with emphasis on data entry, literature searches, and QA...Data
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