Clinical Research Specialist jobs in Chicago, IL
Recently Added Clinical Research Specialist 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 Physician
- GenHarp Clinical Solutions
-
Evergreen, IL
FULL_TIME
- The Clinical Research Physician (Principal Investigator) role will be based in Evergreen Park, IL, and is a part-time contract position. This role is hybrid (remote and on-site). Job Duties & Responsi...
- 3 Days Ago
Senior Clinical Research Associate
- OnPoint Clinical Staffing Services
-
Chicago, IL
FULL_TIME
- Job DescriptionSenior CRAResponsibilities include:* All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical t...
- 13 Days 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....
- 4 Days Ago
Clinical Research Regulatory & Quality Specialist
- Insight
-
Chicago, IL
FULL_TIME
- Insight Research Institute is a rapidly growing non profit organization looking to expand its clinical research division at the Insight Hospital and Medical Center in Chicago, IL. We are looking for d...
- 21 Days Ago
Clinical Practice Data Analyst Specialist (Clinical Research Financial Specialist)
- University of Illinois
-
Chicago, IL
FULL_TIME
- Clinical Practice Data Analyst Specialist (Clinical Research Financial Specialist) Hiring Department: Patient Accounting Location: Chicago, IL USA Requisition ID: 1015737 Posting Close Date: 4/29/2024...
- 2 Months Ago
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0 Clinical Research Specialist jobs found in Chicago, IL area
Clinical Research Coordinator
- Medasource
-
Evanston, IL
- Clinical Research Coordinator Location: Evanston, IL Hours: Monday-Friday, standard business hours Required Travel: Some...
- 6/5/2024 12:00:00 AM
Clinical Research Associate, Endocrinology
- Northwestern University
-
Chicago, IL
- Department: MED-Endocrinology Salary/Grade: RES/ Job Summary: The Division of Endocrinology is seeking a full-time Clini...
- 6/4/2024 12:00:00 AM
Clinical Research Assistant II
- University of Chicago
-
Chicago, IL
- Department BSD OBG - Lindau Lab - Special Projects About the Department The Lindau Laboratory at The University of Chica...
- 6/3/2024 12:00:00 AM
Clinical Research Technician
- US Tech Solutions
-
North Chicago, IL
- Duration: 12 months contract Responsibilities: • Review protocols and comply with study-specific activities • Communicat...
- 6/2/2024 12:00:00 AM
Clinical Research Associate
- Piper Companies
-
Chicago, IL
- Piper Companies is currently seeking a Clinical Research Associate (CRA) for an opportunity in Chicago, Illinois (IL). T...
- 6/2/2024 12:00:00 AM
Clinical Research Associate (CRA) - C
- The Fountain Group
-
Des Plaines, IL
- Hello, My name is Alexa, and I am a Recruiter with The Fountain Group. We are a national staffing firm and are currently...
- 6/1/2024 12:00:00 AM
Clinical Research Coordinator 1
- University of Chicago
-
Chicago, IL
- Department BSD MED - Hematology and Oncology - Clinical Research Staff - Cluster 3 About the Department The Section of H...
- 6/1/2024 12:00:00 AM
Clinical Research Coordinator I
- Icon Plc
-
Downers Grove, IL
- At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and ...
- 6/1/2024 12:00:00 AM
About Chicago, Illinois
Chicago (/ʃɪˈkɑːɡoʊ/ (listen), locally also /-ˈkɔː-/), officially the City of Chicago, is the most populous city in Illinois, as well as the third most populous city in the United States. With an estimated population of 2,716,450 (2017), it is the most populous city in the Midwest. Chicago is the principal city of the Chicago metropolitan area, often referred to as Chicagoland, and the county seat of Cook County, the second most populous county in the United States. The metropolitan area, at nearly 10 million people, is the third-largest in the United States, and the fourth largest in North A...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Specialist jobs
$53,394 to $70,406
Chicago, Illinois area prices
were up 0.8% from a year ago
were up 0.8% from a year ago
What does a Clinical Research Specialist do?
Clinical Research Specialist
Prepare and/or coordinate IRB submission and approval of new phase I-III protocols for industry, investigator initiated, and national cooperative group studies in assigned disease area.
March 05, 2023
Requires the Specialist to have at least one year of clinical research experience to ensure adequate knowledge of research and institutional systems to decrease the length of onsite training and increase project productivity.
March 19, 2023