Clinical Research Associate Jobs in Streamwood, IL
Clinical Research Associate, Sponsor Dedicated
- IQVIA Holdings Inc
- Oak Brook, IL (20 miles from Streamwood, IL)
- 1 day ago
- Oak Brook, IL (20 miles from Streamwood, IL)
- 1 day ago
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines....
In Person- Astellas Pharma, Inc.
- Northbrook, IL (18 miles from Streamwood, IL)
- 30+ days ago
- Northbrook, IL (18 miles from Streamwood, IL)
- 30+ days ago
A CSM is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable...
In Person- Fifth Third Bank
- Rolling Meadows, IL (8 miles from Streamwood, IL)
- 90+ days ago
- Rolling Meadows, IL (8 miles from Streamwood, IL)
- 90+ 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...
In PersonDemographic Data for Streamwood, IL
Moving to Streamwood, IL? Find some basic demographic data about Streamwood, IL below.
Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in Streamwood, IL
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in Streamwood, IL offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Research Associate position
- ICH GCP
- Clinical Data Management
- Study Management
- Clinical Monitoring
- Gene Therapy
- Cancer Research
- Biostatistics
- Sample Preparation
- Mortgage Lending
- Scientific Research
- Clinical Trial Management System
- Federal Housing Administration
- Fannie Mae
- Institutional Review Board
- ICH Guidelines
- Drug Development
- Good Clinical Practice
- Site Management
- Biotechnology
- Clinical Operations
- Oncology
- Medical Device Sales
- Clinical Trials
- Clinical Research
- FDA Regulations
- Data Management
- Data Collection
- Standard Operating Procedures
- Health Care
- Collections
- Auditing
- Implementation
- Collaboration
- Reporting
- Documentation
- Verbal Communication
- Data Entry
- Investigation
- Microsoft PowerPoint
- Mentoring
- Policy Development
- Education Experience
- Bachelor's Degree
- Regulations
- Research Skills
- Computer Skills
- Microsoft Word
- Microsoft Office
- Staff Supervision
- Microsoft Excel
- Problem Solving
- Scheduling
- Time Management
- Leadership
- Communication Skills
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