Top Clinical Research Executive jobs in Chicago, 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.
- 1 Day 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 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...
- 13 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
- uic
-
Chicago, IL
FULL_TIME
- Job Summary: The Executive Director, Clinical Health Research Informatics is responsible for supporting organization wide healthcare research by using data science. They provide leadership to data sci...
- 11 Days Ago
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0 Top Clinical Research Executive jobs found in Chicago, 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
Research and Compliance Analyst
- Shirley Ryan AbilityLab
-
Chicago, IL
- By joining our team, you'll be part of our life-changing Mission and Vision. You'll work in a truly inclusive environmen...
- 4/24/2024 12:00:00 AM
Research Technician
- University of Chicago
-
Chicago, IL
- Department BSD BMD - Miao Lab About the Department The Ben May Department for Cancer Research was formally established i...
- 4/24/2024 12:00:00 AM
Research Associate I Education and Healthy Aging Research - Hybrid Office Schedule
- U Of C Norc
-
Chicago, IL
- JOB SUMMARY: NORC at the University of Chicago is seeking a Regular, Full Time Research Associate I tojoin The Bridge in...
- 4/23/2024 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
Research Specialist I
- Loyola University Chicago
-
Maywood, IL
- Job Description Job Description Candidates, please apply directly on our website: https://www.careers.luc.edu/postings/2...
- 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 Study Assistant (Ophthalmology)
- Northwestern University
-
Chicago, IL
- Department: MED-Ophthalmology Salary/Grade: NEX/9 Job Summary: Performs biomedical &/or social-behavioral research by ad...
- 4/21/2024 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 Top Clinical Research Executive jobs
$220,939 to $403,224
Chicago, Illinois area prices
were up 0.8% from a year ago
were up 0.8% from a year ago