Regulatory Clinical Research Coordinator - IRB & Compliance
$29.36 - $42.61 per hourRush University Medical Center
A leading medical research center in Chicago seeks a Clinical Research Regulatory Coordinator 2 to prepare and maintain regulatory documents for clinical trials. The role involves managing workflows throughout the study lifecycle and serving as the primary regulatory contact for various studies. Candidates should have a Bachelor's degree and at least 2 years of clinical experience, with knowledge of relevant regulations and strong organizational skills. This full-time position offers a competitive pay range of $29.36 – $42.61 per hour. #J-18808-Ljbffr Rush University Medical Center
$29.36 - $42.61 per hour
...Medical Center Department: Research Affairs-ResAdm Work... .... Job Summary: The Clinical Research Regulatory Coordinator 2 (CRRC 2) prepares,... ...study lifecycle, including IRB submissions, institutional... ...updates, and documentation of compliance requirements. The CRRC 2...RegulatoryHourly payFull timeContract workWork at officeShift work- Job Title: Clinical Research Coordinator I Location: Maywood-Health Sciences Campus, Loyola University... ..., maintaining efficiency and regulatory compliance across studies conducted at Loyola... ...ongoing communication with the local IRB, federal organizations, affiliate institutions...RegulatoryFull timeWork experience placementWork at officeLocal area
- ...Department BSD SUR - Research Services:... ...influence standard clinical practice. Today,... ...Clinical Research Coordinator 2 (CRC2) is a specialized... ...of compliance, financial, and related... ...PI, sponsor, and IRB under the clinical... ...sponsor, PI, and regulatory specifications....RegulatoryWork experience placement
- ...goal, and our unique research and powerful... ..., human touch. The Clinical Research Coordinator (CRC) will work collaboratively... ...studies and ensure compliance with study review... ...trials operations and regulatory compliance. Review... ...site, sponsor, and IRB for initiation, interim...RegulatoryTemporary workInterim roleLocal area
$50k - $65k
...Department The Office of Clinical Research (OCR) was created to... ...while promoting compliance and human subject protection... ...Subject Protection (IRB); Research Compliance... ...Clinical Research Coordinator I (CRC I) supports... ...visits, data collection, regulatory documentation, and...RegulatoryWork experience placementWork at office$50k - $65k
...neurological training, clinical care, and the basic... ...Aging & Alzheimer's Research Care (HAARC) Center,... ...This Clinical Research Coordinator I (CRCI) provides support... ...data collection and regulatory compliance across studies.**... ...informed consent, relevant IRB approvals, source...RegulatoryContract workWork experience placement$60k - $75k
...Department**BSD OCR - Clinical Research Incubation**About the... ...while promoting compliance and human subject protection... ...data management, and regulatory services to... ...The Clinical Research Coordinator 2 (CRC2) is a specialized... ...documentation (i.e. IRB submissions, educational...RegulatoryWork experience placementWork at office$51.35k - $72.53k
...social-behavioral research study involving... ...& publication & coordinates writing, submission... ...strictly following Good Clinical Practices (GCP) &... ...Review Board (IRB), Food & Drug... ...deadlines and overall compliance with policy and... ...charts or regulatory forms. Aid in negotiation...RegulatoryWork at officeLocal areaFlexible hours- ...healthcare provider in Chicago is seeking a Clinical Research Coordinator to support clinical trials by managing protocols, ensuring compliance, and assisting principal investigators.... ...approach, with the ability to maintain regulatory standards and manage patient...Regulatory
- A leading pediatric healthcare organization in Chicago is seeking a Clinical Research Coordinator to oversee research projects, ensure regulatory compliance, and engage with study participants. Ideal candidates will have a Bachelor's degree and at least two years of relevant...Regulatory
- Rush University Medical Center is seeking a Clinical Research Coordinator III to independently manage clinical research studies in a collaborative... ...environment. This crucial position ensures compliance with regulatory requirements while overseeing recruitment, data entry...Regulatory
- A higher education institution in Maywood seeks a Clinical Research Coordinator I to manage clinical research trials, ensuring regulatory compliance and effective communication with research participants and sponsors. The role requires a Bachelor’s degree and offers a...RegulatoryWork at office
- ...Hospital is seeking a Senior Regulatory Coordinator to manage all regulatory matters... ...regulatory documentation and clinical research protocols. Responsibilities include communicating with IRB, managing submissions, and ensuring compliance with federal guidelines. Competitive...Regulatory
- A leading medical center in Chicago is seeking a Clinical Research Regulatory Coordinator 2 to prepare and manage regulatory documents for clinical research... ...communication skills, and the ability to manage compliance across multiple studies. A master's degree is...RegulatoryFull time
$60k - $85k
A research institution in Chicago is seeking an IRB Coordinator to provide regulatory expertise and support the Department of Surgery. The ideal candidate will educate researchers on human subject research compliance, prepare research protocols, and maintain IRB documentation...Regulatory$75k - $100k
...Clinical Trials/Contracts Manager The Office of Clinical Research (OCR) is dedicated to supporting the infrastructure... ...while promoting compliance and human subject... ...Institutional Review Board (IRB) submissions and... ...account creations, regulatory and compliance monitoring...RegulatoryContract workWork experience placementWork at office$69k - $78k
...Department: IRB Office Salary/Grade: EXS/7 Target hiring... ...direct supervision, the IRB Compliance Analyst ensures that the various research compliance activities and... ...researchers with identifying regulatory agency and good clinical practice requirements surrounding...RegulatoryWork at officeLocal area$69k - $78k
Department: IRB Office Salary/Grade: EXS/7 Target hiring range... ...direct supervision, the IRB Compliance Analyst ensures that the various research compliance activities and... ...researchers with identifying regulatory agency and good clinical practice requirements surrounding...RegulatoryWork at officeLocal areaFlexible hoursWeekend work- ...The Department The Office of Clinical Research (OCR) is dedicated to... ...enterprise while promoting compliance and human subject protection... ...Summary The Clinical Research Coordinator 2 - Ophthalmology (CRC2) works... ...of research documentation (IRB submissions, educational materials...Work experience placementSecond jobWork at office
- Position: Clinical Research Coordinator III Location: Chicago, IL Job Id: 1152 # of Openings: 1 Clinical... ...limited to: Sponsor-provided and IRB-approved Protocol Training All... ...clinical trials experience preferred. Regulatory research experience is a plus. Credentials...Regulatory
- * Coordinate all aspects of conducting clinical trials including: screening, enrollment, subject... ...informed consent, relevant IRB approvals, source... ...conduct the study and retain research subjects.* Understands protocols... ...investigator, and regulatory agency specifications.* Prepare...Regulatory
- ...aspects of conducting clinical trials including... ...other clinical research staff.* Collects,... ...(CROs), and regulatory authorities related... ...clinical trial.* Coordinates the conduct of the... ...information and compliance with federal regulations... ..., relevant IRB approvals, source...RegulatoryContract workWork at office
$50k - $75k
Clinical Research Coordinator - University of Illinois Chicago, Chicago, IL, USA... ...Institutional Review Board (IRB), Protocol Review Committee... ...to ensure protocol compliance. Act as liaison between physicians... ..., grant sponsors and regulatory agencies to ensure priorities...RegulatoryWork at office- Clinical Research Coordinator I Position Title: Clinical Research Coordinator I Position... ...trials, maintaining compliance with good clinical practice... ..., sponsors, and regulatory agencies; coordinate studies... ...communication with the local IRB, federal organizations, affiliate...RegulatoryFull timeWork experience placementWork at officeLocal area
$50k - $65k
...treatment to conducting research to find promising... ...of future clinical pediatricians, subspecialists... ...Clinical Research Coordinator (CRC) 1 in... ...sponsor, PI, and regulatory agency specifications. Ensures compliance with federal regulations... ...consent, relevant IRB approvals, source...RegulatoryWork experience placementWork at office$50k - $65k
...- Hematology and Oncology - Clinical Research Staff - Cluster 1 Department... ...Summary The Clinical Research Coordinator I provides support to the... ...informed consent, relevant IRB approvals, source documentation... ..., primary investigator, and regulatory agency specifications....RegulatoryWork experience placement$29.36 - $42.61 per hour
...Medical Center Department: ER Research Recruit - Gottlieb Work... ...61 per hour Summary The Clinical Research Coordinator III (CRC III)... ...responsible for ensuring compliance with regulatory and institutional requirements... ...and applies NIH, FDA, and IRB rules for high‐complexity...RegulatoryHourly payFull timeLocal areaShift work$46.28k - $75.67k
...study team in the implementation, coordination, and conduct of clinical research activities. Adheres to the service... ...preparation and maintenance of all regulatory documents required by sponsors and... ...necessary study documents for IRB and/or sponsor review. Assists clinical...RegulatoryFlexible hours$70k - $85k
...CCC - Network Oncology Research Support Job Summary The Senior Clinical Research Coordinator (Sr CRC) is a... ...their conduct to ensure compliance with federal and institutional... ...documentation, i.e., IRB submissions,... ...requirements. Maintain regulatory documentation. Assist...RegulatoryWork experience placement$46.28k - $75.67k
...in medical technology, research and family-friendly design... ...and maintenance of all regulatory documents required by sponsors... ...study documents for IRB and/or sponsor review.* Assists clinical research personnel in... ...participants and families.* Coordinates reimbursement for study...RegulatoryHourly payFull timePart time
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