Clinical Research Associate Jobs in Chicago, IL
A Clinical Research Associate (CRA) plays a pivotal role in the biotechnology industry, overseeing various aspects of clinical trials. These include designing, implementing, and monitoring clinical trials, ensuring data integrity, verifying case report forms, providing progress reports, and ensuring compliance with protocols and regulatory requirements. CRAs play a crucial role in the development, testing, and approval of new products in the biotechnology industry by managing the clinical trials that prove their safety and efficacy.
Important skills for a CRA include strong communication and organizational abilities, keen attention to detail, knowledge of clinical practices, and analytical skills. CRAs also need to be proficient in using specialized software for data analysis and trial management. Certifications such as Certified Clinical Research Associate (CCRA) or Certified Clinical Research Professional (CCRP) are typically required. Prior to becoming a CRA, individuals might have roles such as Clinical Research Coordinator, Clinical Trial Assistant, or Research Nurse, gaining necessary experience in managing clinical trials and working in a research setting.
form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with protocols, GCP (Good Clinical...
skills Ability to work independently and manage multiple priorities Proficiency in using clinical trial management systems and other relevant software Certifications: Certified Clinical Research Associate...
In-depth working knowledge of FDA regulations, ICH guidelines, and GCP governing the conduct of clinical trials. Familiarity with pharmaceutical and medical terminology....
skills Ability to work independently and manage multiple priorities Proficiency in using clinical trial management systems and other relevant software Certifications: Certified Clinical Research Associate...
Clinical Practices (ICH-GCP) Investigates research compliance breaches, gathers relevant information, assesses impact, determines steps to mitigate risk, and reports findings Documents detailed compliance...
- Rolling Meadows, IL (22 miles from Chicago, IL)
- 14 days ago
- Rolling Meadows, IL (22 miles from Chicago, IL)
- 14 days ago
Make banking a Fifth Third better We connect great people to great opportunities. Are you ready to take the next step? Discover a career in banking at Fifth Third Bank. GENERAL FUNCTION: Performs...
The Comprehensive Cancer Center is comprised of over 190 faculty members from twenty departments with members currently being awarded over $47 million in total direct costs in peer-reviewed cancer research...
Demonstrated knowledge of Good Clinical Practices and Good Documentation Practices. Demonstrated knowledge of current NIH and/or FDA regulations and guidelines related to clinical research....
Demonstrated knowledge of Good Clinical Practices and Good Documentation Practices. Demonstrated knowledge of current NIH and/or FDA regulations and guidelines related to clinical research....
Now Hiring: Compliance Program Manager - CRA Focus | Chicago, IL (Hybrid/On-site) Are you a strategic thinker with a passion for regulatory excellence and community impact? Join a respected...
Location: Chicago, Illinois Business Unit: Rush Medical Center Hospital: Rush University Medical Center Department: Cancer Center-Res Fac Work Type: Full Time (Total FTE between 0.9 and 1.0)...
form, and determine if clinical trial/study subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/study safety, in keeping with protocols, GCP (Good Clinical...
GCP and other) standards and guidelines....
GCP and other) standards and guidelines....
Participates in study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports....
Demographic Data for Chicago, IL
Moving to Chicago, IL? Find some basic demographic data about Chicago, IL below.
Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in Chicago, IL
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in Chicago, IL offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Research Associate position
- Compliance Monitoring
- Mortgage Lending
- Fannie Mae
- Sample Preparation
- ICH GCP
- Study Management
- Clinical Monitoring
- Institutional Review Board
- Clinical Trial Management System
- Cancer Research
- Gene Therapy
- Good Clinical Practice
- ICH Guidelines
- Medical Affairs
- Biology
- Scientific Research
- Drug Development
- Physiology
- Site Management
- Biotechnology
- Clinical Trials
- Neuroscience
- Clinical Operations
- Clinical Research
- Oncology
- Medical Device Sales
- FDA Regulations
- Data Collection
- Patient Care
- Standard Operating Procedures
- Data Management
- Technical Writing
- Collections
- Auditing
- Written Communication
- Documentation
- Education Experience
- Investigation
- Collaboration
- Reporting
- Inventory Management
- Bachelor's Degree
- Policy Development
- Regulations
- Problem Solving
- Research Skills
- Microsoft Office
- Microsoft Excel
- Teamwork
- Time Management
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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