Clinical Research Coordinator jobs in Illinois
Clinical Research Coordinator organizes research information for clinical projects. Selects and observes subjects and assists with data analysis and reporting. Being a Clinical Research Coordinator oversees experiment scheduling and collection of data. Requires a high school diploma or equivalent. Additionally, Clinical Research Coordinator typically reports to a supervisor or manager. The Clinical Research Coordinator works under moderate supervision. Gaining or has attained full proficiency in a specific area of discipline. To be a Clinical Research Coordinator typically requires 1-3 years of related experience. (Copyright 2024 Salary.com)
Recently Added Clinical Research Coordinator jobs
Clinical Research Coordinator III
- DM Clinical Research
-
Chicago, IL
FULL_TIME
-
Clinical Research Coordinator III
A CRC III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. To ensure study enrollment meets or exceeds Sponsors' expectations. To ensure company goals are achieved on a timely basis.
DUTIES & RESPONSIBILITIES- Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
- Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
- Sponsor-provided and IRB-approved Protocol Training
- All relevant Protocol Amendments Training
- Any study-specific Manuals Training, as applicable
- Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
- Conducting and overseeing study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.
- Adherence to ALCOA-C Standards with all the relevant clinical trial documentation.
- Completing and overseeing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
- Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
- Demonstrated understanding, implementation and supervision of protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration, and laboratory kit inventory for assigned protocols.
- Liaising with the Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives for assigned protocols.
- Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s)
- Maintaining a working knowledge of the recruitment and retention process for their assigned protocol(s) at their respective site(s).
- Ability to train and mentor site staff, as needed
- Supervise visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s)
- Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
- Maintaining a working knowledge of the most recent versions of the Study Protocols, Informed consents, Study Manuals, and all the other relevant study-related documents that are utilized and implemented for the assigned protocols at their respective site(s).
- Maintaining a working knowledge of Study Participants’ Scheduling, Visit Tracking, Stipends and Transportation by liaising with the Administrative team.
- Maintaining a working knowledge of the Essential Clinical Trial Documents and maintenance of the Investigator Site Binders for their assigned protocol(s) at their respective site(s)
- Oversee reporting of all Adverse and Serious Adverse Events and any other relevant Safety Information to the appropriate authorities per internal company guidelines, Sponsor, IRB, and ICH-GCP Guidelines.
- Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
- Being prepared for and available at all required company meetings.
- Submitting required administrative paperwork per company timelines.
- Occasionally attending out-of-town Investigator Meetings
- Conduct patient consent discussions and ensure comprehension of medical procedures, risks, benefits, and alternatives
- Provide clear explanations of study protocols and ensure patients' understanding before obtaining their consent
- Facilitate effective communication between patients, healthcare providers, and research staff
- Any other matters as assigned by management
KNOWLEDGE & EXPERIENCE
Education:- High School Diploma or equivalent required
- Bachelor's degree preferred
- Foreign Medical Graduates preferred
- Minimum of 5 years experience in Clinical Research
- Supervisory experience preferred
- Wide therapeutic range of clinical trials experience preferred
- Regulatory research experience is a plus
- ACRP or equivalent certification is preferred
- Goals-driven while continuously maintaining quality.
- Must be detailed-oriented, proactive, and able to take initiative.
- Must have strong written and communication skills.
- Must have excellent customer service skills.
- Proficient communication and comprehension skills both verbal and written in the English language are required.
- Proficient Bi-lingual (English/Spanish) communication and comprehension skills both in verbal and written are preferred.
- 2 Months Ago
Clinical Research Coordinator
- Revival Research Institute, LLC
-
Elgin, IL
FULL_TIME
- Unique opportunity to make an Impact in the healthcare industry…Revival Research Institute, LLC was established in 2015, and headquartered in the Metro Detroit Region, and has been growing ever since....
- 2 Days Ago
Clinical Research Coordinator 228636
- Medix™
-
Downers Grove, IL
FULL_TIME
- We are looking to add a full time onsite CRC to our growing team. This person will be working at a handful of sites in and or around the Downers Grove area. We are open to minimal coordinating experie...
- 2 Days Ago
Clinical Research Coordinator - 225515
- Medix™
-
Chicago, IL
FULL_TIME
- Clinical Research Coordinator Opportunity in Chicago, IL(60611)Medix is currently seeking experienced Research Professionals wanting to grow their career in the Clinical Research Field. If you are int...
- 2 Days Ago
Clinical Research Coordinator 1
- University of Chicago
-
Chicago, IL
FULL_TIME
- Department BSD MED - Hospital Medicine - Clinical Research Staff - CCP About the Department Hospital Medicine is a rapidly growing field within internal medicine where physicians, called ‘Hospitalists...
- 3 Days Ago
Clinical Research Coordinator
- University of Illinois Hospital
-
Chicago, IL
OTHER
- Position SummaryThis position manages and coordinates the timely handling of all components of clinical research protocols, including pre and post research activities, internal and external to the cli...
- 3 Days Ago
Clinical Research Coordinator jobs at Popular Companies
Clinical Research Coordinator
- Advarra
-
- About Advarra: Advarra makes clinical research safer, smarter, and faster. Our integrated solutions help safeguard trial...
- 6/11/2024 12:00:00 AM
Clinical Research Coordinator
- Advarra
-
- About Advarra: Advarra makes clinical research safer, smarter, and faster. Our integrated solutions help safeguard trial...
- 6/11/2024 12:00:00 AM
Clinical Research Coordinator
- Sanford Health
-
Fargo, ND
- Careers With Purpose Sanford Health is one of the largest and fastest-growing not-for-profit health systems in the Unite...
- 6/10/2024 12:00:00 AM
Clinical Research Coordinator
- Danbury Health Systems
-
Norwalk, CT
- Clinical Research Coordinator, Norwalk, CT Full-time, 40 hours; 8:30 am - 5:00 pm Nuvance Health has a network of conven...
- 6/10/2024 12:00:00 AM
Clinical Research Coordinator
- CARLE
-
Peoria, IL
- Promotes good clinical practices in the conduct of clinical investigations by possessing an in-depth knowledge of federa...
- 6/9/2024 12:00:00 AM
Clinical Research Coordinator
- CARLE
-
Urbana, IL
- The Clinical Research Coordinator (CRC) is a specialized research professional that facilitates and coordinates the dail...
- 6/8/2024 12:00:00 AM
Clinical Research Coordinator
- Sanford Health
-
Sioux Falls, SD
- Careers With Purpose Sanford Health is one of the largest and fastest-growing not-for-profit health systems in the Unite...
- 6/8/2024 12:00:00 AM
Clinical Research Coordinator
- Hackensack Meridian Health
-
Nutley, NJ
- Overview: Our team members are the heart of what makes us better. At Hackensack Meridian Health we help our patients liv...
- 6/7/2024 12:00:00 AM
About Illinois
Illinois (/ˌɪlɪˈnɔɪ/ (listen) IL-ih-NOY) is a state in the Midwestern and Great Lakes region of the United States. It has the fifth largest gross domestic product (GDP),
the sixth largest population, and the 25th largest land area of all U.S. states. Illinois is often noted as a microcosm of the entire United States. With Chicago in northeastern Illinois, small industrial cities and immense agricultural productivity in the north and center of the state, and natural resources such as coal, timber, and petroleum in the south, Illinois has a diverse economic base, and is a major transportation hu...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Coordinator jobs
$61,735 to $83,240
Most Popular Cities in Illinois for Clinical Research Coordinator Jobs
What does a Clinical Research Coordinator do?
Clinical Research Coordinator in Rock Hill, SC
A clinical research coordinator coordinates the clinical trials under the guidance of the principal investigator.
October 22, 2019
Clinical Research Coordinator in Binghamton, NY
However, many people start working in research with no experience and can receive on-the-job training and experience.
November 18, 2019
Clinical Research Coordinator in Portsmouth, NH
With an experienced coordinator, just as with an inexperienced one, it’s the same.
December 11, 2019