Top 32 Assistant clinical research coordinator Jobs in Chicago Il

Clinical Research Coordinator Assistant
Insight —Chicago, IL
- English
- Mid-level
- Travel
- Disability insurance
- Health insurance
Quick Apply
Clinical Research Coordinator I - Oral Health Research Staff
The University of Chicago —Chicago, IL
- $50,000 - $65,000 a year
- Full-time
- Background check
- Dental office
- Inventory control
- Health insurance
- Paid time off
Research Coordinator-Cardiology
Endeavor Health —Glenview, IL
- $24.86 - $37.29 an hour
- Full-time
- Mid-level
- High school diploma or GED
- Bachelor's degree
- Free parking
- Wellness program
Clinical Research Coordinator 3
The University of Chicago —Chicago, IL
- $65,000 - $80,000 a year
- Full-time
- Background check
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Paid time off
3d
Clinical Coordination Assistant
CCRM Fertility —Chicago, IL
- $22 - $24 an hour
- Full-time
- BLS Certification
- Office
- High school diploma or GED
- Commuter assistance
- Health savings account
Quick Apply
Clinical Research Assistant
University Retina —Lemont, IL
- $21.00 - $23.50 an hour
- Full-time
- Microsoft Outlook
- Mid-level
- High school diploma or GED
- Health savings account
- AD&D insurance
Department Assistant (On-site)
DePaul University —Chicago, IL
- $18.70 - $24.21 an hour
- Full-time
- Microsoft Word
- Background check
- Spanish
- Paid holidays
- Health insurance
Research Coordinator - Surgery Research
Endeavor Health —Evanston, IL
- $24.86 - $37.29 an hour
- Full-time
- Surgery
- Computer literacy
- Mid-level
- Free parking
- Wellness program
Patient Entry Team Member
Chicago Cosmetic Surgery and Dermatology —Chicago, IL
- Overtime
- Surgery
- Computer literacy
- HIPAA
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator
Genesis Orthopedics & Sports Medicine —Oak Brook, IL
- Full-time
- Mid-level
- In-person
- Communication skills
- Opportunities for advancement
Quick Apply
Clinical Research Coordinator
Apex Medical Research —Chicago, IL
- Email
- Nursing
- Medical office experience
- Mid-level
Administrative Assistant
Flourish Research —Chicago, IL
- $20 - $23 a year
- Full-time
- Writing skills
- Administrative experience
- Analysis skills
- Paid holidays
- Disability insurance
Quick Apply
Clinical Research Coordinator III - Team Lead
Insight —Chicago, IL
- Weekends as needed
- Nursing
- Hospital
- Computer literacy
Quick Apply
Senior Care Coordinator, Therapeutic Services
The University of Chicago —Chicago, IL
- $60,000 - $80,000 a year
- Full-time
- Background check
- Microsoft Excel
- Microsoft Outlook
- Health insurance
- Paid time off
Research Assistant/Phlebotomist
Merieux NutriSciences —Addison, IL
- $22 - $24 an hour
- Full-time
- Vital signs
- OSHA
- Bachelor of Science
- Health insurance
- Dental insurance
11d
Senior Project Coordinator - Legs & Walking, Full-Time
Shirley Ryan AbilityLab —Chicago, IL
- $61,800 - $103,000 a year
- Full-time
- Management
- Customer service
- Word processing
Quick Apply
8d
Senior Clinical Research Coordinator
University of Illinois —Chicago, IL
- $60,000 - $77,000 a year
- Customer service
- 5 years
- Master's degree
- Health insurance
- Dental insurance
10d
Dental Assistant
The University of Chicago —Chicago, IL
- $21.63 - $26.44 an hour
- Weekends as needed
- Hybrid work
- CDL B
- Background check
- Dental office
- Health insurance
- Paid time off
Clinical Research Nurse
Loyola University Chicago —Maywood, IL
- $36.06 - $40.87 an hour
- Full-time
- Nursing
- RN License
- Computer literacy
Manager Research Operations - Anatomy & Cell Biology - Full-time
Hospital: Rush University Medical Center —Chicago, IL
- $32.00 - $46.44 an hour
- 8 hour shift
- 5 years
- Word processing
- Master's degree
2d

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Clinical Research Coordinator Assistant

Insight -
Chicago, IL

Quick Apply

Job Details

Benefits

Disability insurance
Health insurance
Dental insurance
Vision insurance
Life insurance
Paid sick time

Qualifications

Medical software
Spreadsheets
Regulatory compliance
Medical terminology

Full Job Description

WE ARE INSIGHT
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.

The Clinical Research Coordinator (CRC) Assistant will work collaboratively with a multi-institutional team. The CRC assistant will support the CRC, administrative staff and principal investigators, assist the communications between sponsor and institute, oversee details of clinical studies and ensure compliance with study review board and clinical research regulations. The CRC assistant can be part of multiple research projects and should have the ability to multi-tasks.

Duties:

Develops and maintains knowledge and proper skills to comply with the protocol, federal regulatory requirements and internal SOPs
Prepare and attend study meetings.
Performs study start-up duties including the production of a recruitment tool, and progress notes, as well as phone screening patients and identifying participants for trials on site
Proactively develops and executes recruitment plans that meet and exceed enrollment goals
Performs study start-up duties including the production of a recruitment plan, recruitment tool, and progress notes, as well as phone screening participants.
Maintains proper skills to update databases, complete participant reimbursement, capture referral source of participants, and create calls lists to promote recruitment.
Creates and updates source documents/progress notes, and collects study data via source documents/progress notes as required by the protocol.
Performs technical requirements of the study protocol, i.e., lab work (phlebotomy and processing), blood pressure, electrocardiograms, pulmonary function testing, allergy testing, urine/serum pregnancy testing, strep throat screening, or any procedure necessary for the protocol as ordered by the investigator or specified by a protocol
Performs continuous reviews of the inclusion and exclusion criteria for each participant during the trial for their trials as well as peer review of inclusion and exclusion for trials
Documents laboratory data and adverse reactions, presents this information to an investigator in a timely manner, and immediately notifies investigators, the Institutional Review Board and sponsor of any serious adverse events
Builds and maintains strong relationships with Investigators and provides ongoing communication about trial status and participants
Dispenses study medication at the direction of the Investigator
Maintains communication with the monitor from the sponsoring company through telephone contact, written communication and on-site visits
Enters visit data in the Electronic Data Capture (EDC) or Case Report Forms (CRF) within timelines provided by sponsor
Addresses all queries or data clarifications within the time period specified by the sponsor
Meets with the Clinical Research Associate at each scheduled monitoring visit and is available to complete queries or data clarifications in a timely manner during these visits
Reports protocol violations and significant deviations to the CRCs and the investigators.
Establishes relationships with participants, and participates through ongoing patient education regarding the clinical trial process and provides specific trial information to the participant as well as conducting the informed consent process
Assists other staff members at the site as determined by the needs and priorities of the organization and as time and abilities permit
Anticipates possible problems and resolutions with job responsibilities as these responsibilities apply to our mission statement

Requirements

Education

Degree in health-related field/life science with minimum one year experience in clinical research
- Clinical research certification GCP and IATA certification are required (or willing to obtain them within the first month of assignment).

Basic Skills:

Medical terminology and knowledge of disease processes
Working knowledge of clinical research design and regulatory requirements
Excellent interpersonal, verbal, and written communication skills.
Organized and detail-oriented individual.
Comfortable working in a team environment
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

Behavioral Competencies

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.

Benefits:

Paid Sick Time - effective 90 days after employment.
Paid Vacation Time - effective 90 days after employment.
Health, vision & dental benefits - eligible at 30 days, following the 1st of the following month.
Short and long-term disability and basic life insurance - after 30 days of employment.

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.

Insight is an Equal Opportunity Employer & Values Workplace Diversity!

Quick Apply

Refine Your Search

assistant clinical research coordinator jobs in chicago il

Clinical Research Coordinator Assistant

Clinical Research Coordinator I - Oral Health Research Staff

Research Coordinator-Cardiology

Clinical Research Coordinator 3

Clinical Coordination Assistant

Clinical Research Assistant

Department Assistant (On-site)

Research Coordinator - Surgery Research

Patient Entry Team Member

Clinical Research Coordinator

Clinical Research Coordinator

Administrative Assistant

Clinical Research Coordinator III - Team Lead

Senior Care Coordinator, Therapeutic Services

Research Assistant/Phlebotomist

Senior Project Coordinator - Legs & Walking, Full-Time

Senior Clinical Research Coordinator

Dental Assistant

Clinical Research Nurse

Manager Research Operations - Anatomy & Cell Biology - Full-time

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