- Two years healthcare related field experience or experience in human research.
- Clinical research certification
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Research Coordinator
1 week ago
The University of Chicago Chicago, United StatesDepartment · BSD MED - Infectious Diseases - Chicago Center HIV Elimination - Research · About the Department · The Chicago Center for HIV Elimination (CCHE) is situated within the Biological Sciences Division at the University of Chicago Medicine. CCHE aims to eliminate all new ...
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Research Study Coordinator
4 days ago
Northwestern University Chicago, United StatesCoordinates 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 campu ...
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Research Project Coordinator
3 days ago
Northwestern University Chicago, United StatesThe Department of Surgery is seeking a strong research coordinator to lead project coordination, data collection, and analysis clinical trials and projects within the greater department. This position will support multiple Principal Investigators and surgical specialties. · A pri ...
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Research Project Coordinator
1 week ago
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Research Project Coordinator
6 days ago
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Research Study Coordinator
6 days ago
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Clinic Research Rn Coordinator-neurosurgery
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Northwestern Memorial Healthcare Chicago, United States**Company Description** · At Northwestern Medicine, every patient interaction makes a difference in cultivating a positive workplace. This patient-first approach is what sets us apart as a leader in the healthcare industry. As an integral part of our team, you'll have the opportu ...
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Epi Research Coordinator 1 Grant
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RUSH University Medical Center Chicago, United States**Location**:Chicago, IL · **Hospital**:RUSH University Medical Center · **Department**:Rush Alzheimers Dis Ctr-ResFac · **Work Type**:Full Time (Total FTE between 0. 9 and 1. 0) · **Shift: Shift 1** · **Work Schedule**:8 Hr (8:00:00 AM - 4:30:00 PM) · Travel Required: reliable t ...
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Research Coordinator
1 week ago
University of Chicago Chicago, United StatesDepartment · BSD PED - Hematology, Oncology, and Stem Cell Transplantation - Pediatric Cancer Data Commons: Contracts Management · About the Department · The Biological Sciences Division's 'Data for the Common Good' (D4CG), is a rapidly growing team of experts in medicine, clinic ...
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Research Coordinator
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Advocate Aurora Health Chicago, United StatesDepartment: · 80028 Research - Clinical Trials: Oncology · Status: · Full time · Benefits Eligible: · Yes · Hou · rs Per Week: · 40 · Schedule Details/Additional Information: · On site Monday - Friday business hours · No on-call, no weekends, no holidays · Flexibility ...
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Research Coordinator
1 week ago
Advocate Aurora Health Chicago, United StatesMajor Responsibilities:Performs clinical and administrative coordination of sponsored clinical trials, research protocols/projects, and biospecimen collection studies, as applicable. Provides guidance to physicians, clinical staff and research team m Research Coordinator, Clinica ...
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Research Coordinator
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University of Chicago Chicago, United StatesDepartment · BSD MED - Infectious Diseases - Chicago Center HIV Elimination - Research · About the Department · The Chicago Center for HIV Elimination (CCHE) is situated within the Biological Sciences Division at the University of Chicago Medicine. CCHE aims to eliminate all new ...
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Research Coordinator
2 weeks ago
University of Chicago Chicago, United StatesDepartment · BSD MED - Infectious Diseases - Chicago Center HIV Elimination - Research · About the Department · The Chicago Center for HIV Elimination (CCHE) is situated within the Biological Sciences Division at the University of Chicago Medicine. CCHE aims to eliminate all new ...
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Research Coordinator
1 week ago
The University of Chicago Chicago, United StatesDepartment · BSD PED - Hematology, Oncology, and Stem Cell Transplantation - Pediatric Cancer Data Commons: Contracts Management · About the Department · The Biological Sciences Division's 'Data for the Common Good' (D4CG), is a rapidly growing team of experts in medicine, clin ...
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Research Project Coordinator
6 days ago
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Research Project Coordinator
3 days ago
Northwestern University Evanston, United StatesManages daily operations of a biomedical &/or social-behavioral research study involving multidisciplinary teams of colleagues, sponsors & other external project stakeholders. Monitors study performance, analyzes & review results, & supervises development & implementation of new ...
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Research Coordinator-cardiology
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Edward-Elmhurst Health Glenview, United StatesResearch Coordinator - Cardiology, Heart Failure program · Position Highlights: · - Position: Research Assistant · - Location: Glenbrook Hospital · - Full Time · - Hours: Standard business hours, Mon-Fri, onsite · Job Summary/Functions: · Minimum Formal Education Required: · - Ba ...
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Clinical Research Coordinator
1 week ago
Medix Chicago, United StatesCLINICAL RESEARCH COORDINATOR OPPORTUNITY IN CHICAGO, IL · **MUST HAVE CLINICAL RESEARCH EXPERIENCE** · Clinical Research Coordinator Job Description Coordinates all aspects of the study including recruitment, consent, screening, scheduling, tracking and provides study updates ...
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Clinical Research Coordinator
1 week ago
University of Illinois at Chicago Chicago, United StatesClinical Research Coordinator - DOM - Pulmonary, Breathe Chicago Center · Hiring Department: Medicine, Division of Pulmonary, Breathe Chicago Center · Location: Chicago, IL · Requisition ID:1024848 · Posting Close Date: May 10, 2024 · About the University of Illinois Chicago · UI ...
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Clinical Research Coordinator
1 week ago
Rush Hospital Chicago, United StatesLocation: Chicago, IL · Hospital: RUSH University Medical Center · Department: Cancer Center-Res Fac · Work Type: Full Time (Total FTE between 0.9 and 1.0) · Shift: Shift 1 · Work Schedule: 8 Hr (8:00:00 AM - 5:00:00 PM) · Summary: · The position supports the Office of R ...
Clinical Research Coordinator - Chicago, United States - Insight Hospital and Medical Center
Description
Envisioning and implementing a holistic approach to neurological treatment is our goal, and our unique research and powerful solutions illuminate the path toward greater innovations for the future of healthcare.
Patients and families seeking effective surgical procedures, rehabilitation, and neurological treatment can trust in our highly skilled and renowned surgical team.
As we provide comprehensive services at our state-of-the-art inpatient and outpatient facilities, we remain driven by our basic oath to help patients heal while providing a genuine, human touch.
TheClinical Research Coordinator (CRC)
will work collaboratively with a multi-institutional team.
The CRC will support principal investigators, work as a link between sponsor and institute, oversee details of clinical studies and ensure compliance with study review board and clinical research regulations.
The CRC can be part of multiple research projects and should have the ability to multi-tasks.Duties
Provide technical support and assist Principal Investigators in study design and operations.
Direct, and coordinate clinical trials projects.
Solicits industry trials for potential participation.
Act as a main point of contact for study protocols and coordinate between clinical study team and CRO/Sponsor.
Evaluate protocols and assist in study selection.
Implement and ensure clinical trials operations and regulatory compliance.
Review GCP guidelines, maintain GCP/CITI certification and obtain study-specific required certification for participating study staff.
Manage all clinical trial patients enrolled in studies, discuss protocols and informed consents, and ensure eligibility criteria and recruitment.
Coordinate all study visits including site initiation, study closeout, external audits, and monitoring visits.
Create study-specific source document binders for each study and subject.
Maintain regulatory documents required for study site, sponsor, and IRB for initiation, interim reports, and close-out documentation.
Assign tasks to other members of the research team, ensure they comply with the protocols, and ensure performing all protocol visits, assessments, and procedures.
Maintain databases for all clinical trials.Report adverse events to the Data Safety and Monitoring Board, sponsor, IRB, FDA and all governing bodies.
Submit protocols and amendments to the IRB.
Complete study source documentation, complete study report forms via proposed procedure, maintain proper study close-out and ensure meeting sponsor deadlines.
RequirementsEducation:
Bachelor's degree in health-related field with minimum one year experience as a CRC is required
SOCRA or ACRP certification are preferred.
Basic Skills:
Medical terminology and knowledge of disease processes
Working knowledge of clinical research design and regulatory requirements
Analytical skills to gather and interpret research data.
Excellent interpersonal, verbal, and written communication skills.
Organized and detail-oriented individual.
Comfortable working in a team environment
Capability to work under minimal supervision
Proficient in spreadsheets and clinical research software.
Understand clinical procedures, regulations and be an excellent team player working with physicians, nurses, non-clinical, laboratory and ancillary staff
Capability to meet data deadlines and maintain confidentiality
Ability to travel to INSIGHT local offices when needed
Ability to relate and work effectively with others.
Demonstrated skills in verbal and written English communications for safe and effective patient care and to meet documentation standards.
Proven excellence in patient safety and care.
Friendly, empathetic & respectful.
Reliable in work results, timeliness & attendance.
Ability to relate to and work effectively with a wonderfully diverse populace.
Able to work in a fast-paced, and stressful environment while maintaining positive energy.
Able to work under pressure and in situations that benefit from patience, tact, stamina and endurance.
Detailed oriented, conscientious and committed to precision in work results.
Committed to contributing to a positive environment, even in rapidly changing circumstances.
Is aware of standards and performs in accordance with them.
Able to provide eligibility for employment for any U.S. employer.
Insight Employees are required to be vaccinated for COVID-19 as a condition of employment, subject to accommodation for medical or sincerely held religious beliefs.
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