Top Clinical Research Executive jobs in Skokie, IL
Top Clinical Research Executive plans and directs all aspects of the clinical research function for a healthcare organization. Develops research studies and creates standards and guidelines for clinical research services and programs. Being a Top Clinical Research Executive ensures adherence to SOPs, Good Clinical Practice and FDA regulations. Requires an advanced degree. Additionally, Top Clinical Research Executive typically reports to top management. The Top Clinical Research Executive manages a departmental function within a broader corporate function. Develops major goals to support broad functional objectives. Approves policies developed within various sub-functions and departments. To be a Top Clinical Research Executive typically requires 8+ years of managerial experience. Comprehensive knowledge of the overall departmental function. (Copyright 2024 Salary.com)
Recently Added Top Clinical Research Executive 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.
- Just Posted
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 Months Ago
Clinical Research Coordinator (CRC)
- Center for Clinical and Translational Science
-
Chicago, IL
FULL_TIME
- Clinical Research Coordinator, UIC Center for Clinical and Translational ScienceThe Clinical Research Coordinator works within the CCTS Clinical Research Center and is responsible for managing and coo...
- 12 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...
- 1 Month Ago
Senior Clinical Research Associate (West Coast - Oncology)
- Advanced Clinical
-
Deerfield, IL
FULL_TIME
- ***This position can work remotely anywhere in the United States*** What's in it for YOU? Competitive compensation with comprehensive medical, vision, and dental benefits package 10 paid holidays incl...
- 1 Month Ago
Executive Director, Clinical Health Research Informatics, OPHS
- University of Illinois
-
Chicago, IL
FULL_TIME
- Executive Director, Clinical Health Research Informatics, OPHS Hiring Department: Office of Population Health Sciences Location: Chicago, IL USA Requisition ID: 1024830 Posting Close Date: April 26, 2...
- 10 Days Ago
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0 Top Clinical Research Executive jobs found in Skokie, IL area
Research Recruiter
- SYLVER CONSULTING LLC
-
Evanston, IL
- Job Description Job Description We are looking for a Research Recruiter & Database Developer who has the skills and know...
- 4/24/2024 12:00:00 AM
Clinical Research Coordinator
- GI Associates & Endoscopy Center
-
Glenview, IL
- GI Alliance is seeking an experienced Clinical Research Coordinator. Duties of this position include, but are not limite...
- 4/22/2024 12:00:00 AM
Research Project Coordinator
- Northwestern University
-
Chicago, IL
- Department: MED-Ctr-Dissemination & Implem Salary/Grade: EXS/5 Job Summary: The Center for Dissemination and Implementat...
- 4/22/2024 12:00:00 AM
UX Researcher
- Net2source Inc.
-
Chicago, IL
- Need UX researcher with Healthcare/Medical domain experience. Job Title: UX Researcher Location: Waukesha, WI or Chicago...
- 4/22/2024 12:00:00 AM
Quantitative Researcher
- Durlston Partners
-
Chicago, IL
- Quant Researcher - Systematic Futures HFT - $750K to $1m Hiring an experienced Quant Researcher. This individual will be...
- 4/22/2024 12:00:00 AM
Principal Researcher
- University of Chicago
-
Chicago, IL
- Department Booth Faculty Research - Research Professional About the Department The University of Chicago Booth School of...
- 4/21/2024 12:00:00 AM
Research Analyst 1
- Northwestern University
-
Evanston, IL
- Department: Kellogg GPRL Salary/Grade: EXS/5 Job Summary: The Global Poverty Research Lab (GPRL) is a research center ba...
- 4/21/2024 12:00:00 AM
Quantitative Researcher
- Durlston Partners
-
Chicago, IL
- Quant Researcher - Options Market Making - $600k Hiring an experienced Quant Researcher to develop quantitative models f...
- 4/20/2024 12:00:00 AM
About Skokie, Illinois
According to the 2010 census, Skokie has a total area of 10.06 square miles (26.06 km2), all land. The village is bordered by Evanston to the east, Chicago to the southeast and southwest, Lincolnwood to the south, Niles to the southwest, Morton Grove to the west, Glenview to the northwest, and Wilmette to the north.
The village's street circulation is a street-grid pattern, with major east-west thoroughfare every half-mile: Old Orchard Road, Golf Road, Church Street, Dempster Street, Main Street, Oakton Street, Howard Street, and Touhy Avenue. The major north-south thoroughfares are Skokie B...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Top Clinical Research Executive jobs
$220,939 to $403,224
Skokie, Illinois area prices
were up 0.8% from a year ago
were up 0.8% from a year ago