Top 787 Research Jobs in Evanston Il

Lead Clinical Research Coordinator
Folio Clinical Research —Skokie, IL
- $65,000 - $85,000 a year
- 8 hour shift
- Background check
- 5 years
- Microsoft Office
- Health insurance
- Dental insurance
Quick Apply
Seasonal Employee-Research
Endeavor Health —Evanston, IL
- $17.05 - $23.85 an hour
- Part-time
- Hospital
- High school diploma or GED
- In-person
10d
Research Assistant-Pathology
Endeavor Health —Evanston, IL
- $18.84 - $27.32 an hour
- Full-time
- High school diploma or GED
- Bachelor's degree
- Hospital experience
- Free parking
- Wellness program
Research Assistant-Dermatology
Endeavor Health —Skokie, IL
- $18.84 - $27.32 an hour
- Full-time
- High school diploma or GED
- Clinic
- Bachelor's degree
- Free parking
- Wellness program
Research Assistant-Endocrinology
Endeavor Health —Skokie, IL
- $18.84 - $27.32 an hour
- Full-time
- High school diploma or GED
- Bachelor's degree
- Hospital experience
- Free parking
- Wellness program
Clinical Research Assistant /Pharmacy Tech
Cardiovascular Associates of America —Chicago, IL
- Full-time
- Ability to walk for extended periods
- Computer literacy
- Mid-level
Quick Apply
12d
Research Assistant-Genetics
Endeavor Health —Evanston, IL
- $18.84 - $27.32 an hour
- Full-time
- Master's degree
- Bachelor's degree
- Python
- Free parking
- Wellness program
Library and Research Analyst
Harbor —Chicago, IL
- Full-time
- Remote
- Microsoft Excel
- Microsoft Outlook
- Mid-level
Quick Apply
11d
Research Analyst
Sylver Consulting —Evanston, IL
- Full-time
- In-person
- Entry level
Research Coordinator-Endocrinology
Endeavor Health —Skokie, IL
- $24.86 - $37.29 an hour
- Full-time
- Microsoft Word
- Microsoft Excel
- Patient monitoring
- Free parking
- Wellness program
Research Assistant
Lincoln Park Zoological Society —Chicago, IL
- $22.00 - $24.75 an hour
- Weekends as needed
- Hybrid work
- Current TB test
- Office
- Bachelor's degree
- Free parking
- 403(b) matching
Quick Apply
Research Coordinator-Anesthesia
Endeavor Health —Evanston, IL
- $24.86 - $37.29 an hour
- Full-time
- Mid-level
- High school diploma or GED
- Bachelor's degree
- Free parking
- Wellness program
Epi Research Assistant
Hospital: Rush University Medical Center —Chicago, IL
- $17.63 - $27.77 an hour
- 8 hour shift
- Hospital
- HIPAA
- English
Clinical Research Assistant
Ann & Robert H. Lurie Children’s Hospital of Chicago —Streeterville, IL
- $19.50 - $30.23 an hour
- Full-time
- Spanish
- English
- High school diploma or GED
- 403(b) matching
- Paid parental leave
Research Associate-Cancer Biology
Endeavor Health —Evanston, IL
- $24.86 - $37.29 an hour
- Full-time
- Microsoft Word
- Microsoft Excel
- Writing skills
- Free parking
- Wellness program
Research Assistant
Apex Medical Research —Chicago, IL
- Email
- Office
- Entry level
Climate Scientist - AI Trainer
DataAnnotation —Schaumburg, IL
- $40 - $60 an hour
- Part-time
- Remote
- Computer Science
- English
- Mid-level
- Flexible schedule
Quick Apply
Director, Insights & Revenue Growth Management
High Liner Foods —Chicago, IL
- Sales
- 5 years
- Merchandising
- Dental insurance
- Vision insurance
R&D Food Scientist - Product Development
NORTH AMERICAN HERB & SPICE —Lake Forest, IL
- $60,000 - $80,000 a year
- 8 hour shift
- Ability to walk for extended periods
- Mid-level
- Microsoft Office
- Health insurance
- Dental insurance
Quick Apply
Principal R&D Engineer
Hoerbiger —Waukegan, IL
- $106,682 - $160,023 a year
- Full-time
- 5 years
- Mentoring
- Senior level
- Health savings account
- Paid holidays

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Lead Clinical Research Coordinator

Folio Clinical Research -
Skokie, IL

Quick Apply

Job Details

Full-time
$65,000 - $85,000 a year

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance

Qualifications

Optimizing workflow processes
Data integrity assurance
Clinical research methods
Clinical research
Presentation software
Research ethical considerations
Phlebotomy
Medical software
Operations coordination
FDA 21 CFR Part 11
Phlebotomy specimen handling
Microsoft Office
Patient safety
Data quality management
Data integrity and documentation
ICH guidelines
Clinical research compliance
Bachelor's degree
Continuous improvement
Health information data integrity
Quality improvement
Research compliance clinical trial records management
Clinical trials
Research regulatory compliance
Clinical quality assurance standards
Clinical research documentation
Achieving project delivery timelines
Document management systems
Medical terminology
Project stakeholder communication

Full Job Description

Job description

Folio Clinical Research

Job: Lead Clinical Research Coordinator

Location: Skokie, IL (5x a week)

About Folio Clinical Research

Folio Clinical Research is a leading urologic research network treating urologic cancers, urinary stones, Peyronie’s disease, sexual and erectile dysfunction (ED), low testosterone, prostate disorders, urinary incontinence, and more. We partner with leading physician practices to create a cohesive, quality-oriented clinical culture, facilitating best practice sharing across our platform. Our affiliated practices gain access to a broad suite of clinical trials, providing significant benefits to both physicians and patients.

Position Overview

The Lead Clinical Research Coordinator (CRC) works directly under the supervision of the Principal Investigator (PI) to manage all aspects of clinical trial activities. The CRC is essential in facilitating and coordinating daily clinical trial activities, ensuring compliance, quality, and efficiency throughout the trial process. This role involves direct collaboration with the PI, sponsors, and other key stakeholders. The CRC will interact with patients during the recruitment and screening process. The CRC will also facilitate the informed consent process and provide ongoing participant support as needed.

About You:

Experienced Clinical Research Leader: You have a proven track record in managing clinical research operations, from feasibility assessments to study close-out.

Operational Expertise: You have deep experience managing day-to-day research site operations, ensuring adherence to protocol and regulatory standards

Mentorship Skills: You have training experience and can successfully collaborate with Principal Investigators, particularly those with minimal research experience.

Proactive Problem Solver: You always plan ahead and are proactive about having contingency strategies in place.

Business Acumen: You execute with a sense of urgency, maintaining a keen focus on both research objectives and business outcomes.

Commitment to Quality and Timeliness: You manage study timelines without compromising on quality.

Passion for Innovation: You are dedicated to bringing life-altering treatments to market, driven by patient outcomes.

Effective Communicator: You communicate clearly and regularly, keeping all stakeholders informed and ensuring a smooth study.

Self-Driven: You thrive with minimal supervision, taking ownership and responsibility for your deliverables.

Key Responsibilities:

Regulatory and Institutional Compliance: Support the Principal Investigator and relevant departments to ensure all clinical research activities comply with federal regulations, institutional policies, and sponsor requirements.

Documentation Management: Maintain secure and accurate storage of all study documents, including consent forms, case report forms, and investigational material records, in compliance with both sponsor and institutional requirements.

Study Oversight: Support the PI in ensuring the study meets compliance standards, including Institutional Review Board (IRB) approvals, health and safety requirements, conflict of interest disclosures, and adherence to financial terms.

Stakeholder Coordination: Maintain regular and effective communication with Sponsors, Contract Research Organizations (CROs), and internal team members (e.g., Investigators, Nurses, Medical Assistants) to facilitate study progress.

Meeting Participation: Engage in Site Qualification Visits (SQVs), Site Initiation Visits (SIVs), Interim Monitoring Visits (IMVs), and other key study meetings as required.

Problem-Solving and Adaptation: Identify and anticipate potential obstacles to study timelines or deliverables, offering creative solutions to maintain momentum and study integrity.

Inventory and Equipment Management: Manage study-specific inventory, including identification, ordering, calibration, and secure storage of equipment required for the study.

Qualifications:

Minimum of five years of Clinical Research Coordinator experience.
Experience with various Electronic Data Capture (EDC), Clinical Trial Management Systems (CTMS), and electronic Trial Master File (eTMF) systems.
Comprehensive understanding of urology and other associated therapeutic areas, medical terminology, to effectively execute clinical trials.
Deep knowledge of ICH-GCP, and regulatory requirements, with the ability to implement these effectively throughout the clinical trial.
Experience with data management processes, ensuring the accuracy and completeness of data collection, entry, and reporting, in line with Good Clinical Data Management Practices (GCDMP).
Experience ensuring and prioritizing patient safety and data integrity, embodying a commitment to the ethical conduct of clinical trials.
Experience maintaining the highest quality standards, while focusing on ongoing process improvements that lead to enhanced clinical trial efficiency and compliance.
Excellent interpersonal communication, both written and verbal. Can easily interface with team members and external stakeholders. Proven ability to develop positive relationships with internal teams, physicians, and external partners.
Strong attention to detail, and ability to handle multiple tasks simultaneously in a dynamic research environment.
Strong computer skills (MS Office, M PowerPoint, etc.) and software experience (CTMS, eTMF, EDC, IXRS, RTSM, etc.)
Ability to prioritize tasks, effectively manage time, and allocate resources efficiently to meet tight study deadlines.
Bachelor's degree or equivalent combination of education/experience in science or health-related field.

Any data provided as a part of this application will be stored in accordance with our Policy.

Folio Clinical Research is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

Job Type: Full-time

Pay: $65,000.00 - $85,000.00 per year

Benefits:

Health insurance
Dental insurance
Vision insurance
Paid time off

Medical Specialty:

Urology/oncology

Schedule:

8 hour shift
Monday to Friday

Education:

Bachelor's (Preferred)

Experience:

CRC: 5+ years (Required)

Work Location: In person

Job Type: Full-time

Pay: $65,000.00 - $85,000.00 per year

Benefits:

401(k)
Dental insurance
Health insurance
Paid time off
Vision insurance

Application Question(s):

Will you now or in the future require sponsorship for employment visa status (e.g., H-1B, TN, etc.) to work in the United States?

Education:

Bachelor's (Preferred)

Experience:

Clinical Research Coordinating: 5 years (Preferred)
ICH-GCP: 5 years (Preferred)
EDC, CTMS, & eTMF: 5 years (Preferred)

Location:

Skokie, IL 60077 (Required)

Work Location: In person

Quick Apply

Refine Your Search

research jobs in evanston il

Lead Clinical Research Coordinator

Seasonal Employee-Research

Research Assistant-Pathology

Research Assistant-Dermatology

Research Assistant-Endocrinology

Clinical Research Assistant /Pharmacy Tech

Research Assistant-Genetics

Library and Research Analyst

Research Analyst

Research Coordinator-Endocrinology

Research Assistant

Research Coordinator-Anesthesia

Epi Research Assistant

Clinical Research Assistant

Research Associate-Cancer Biology

Research Assistant

Climate Scientist - AI Trainer

Director, Insights & Revenue Growth Management

R&D Food Scientist - Product Development

Principal R&D Engineer

I want to receive the latest job alert for research in evanston il

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