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.
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....
Senior Clinical Research Associate - Oncology Phase 1 - Midwest
- Chicago, IL
- 1 day ago
- Chicago, IL
- 1 day ago
What you will be doing: The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and...
at Syneos Health LLC in Chicago, Illinois, United States Job Description Description Senior Clinical Research Associate I Syneos Health is a leading fully integrated biopharmaceutical solutions organization...
Senior Clinical Research Associate
- Deerfield, IL (21 miles from Chicago, IL)
- 4 days ago
- Deerfield, IL (21 miles from Chicago, IL)
- 4 days ago
Responsibilities: Ensure clinical trials are conducted in compliance with protocol/amendment(s), with ICH GCP, SOPs and with applicable regulatory requirements in the assigned countries and sites Ensure...
Clinical Research Associate - Oncology Early Development - Central
- Chicago, IL
- 8 days ago
- Chicago, IL
- 8 days ago
Have an in-depth knowledge of Good Clinical Practice, ICH guidelines and local regulatory requirements....
- Rosemont, IL (13 miles from Chicago, IL)
- 11 days ago
- Rosemont, IL (13 miles from Chicago, IL)
- 11 days ago
**You're the right fit if:** + You've acquired 2+ years of experience as a Clinical Research Associate (CRA), ideally within the medical device industry, including experience managing clinical trials...
Responsibilities of the Clinical Research Associate Oversee the development and execution of the clinical trial plans and protocols for Phase I-IV Maintain documentation and data evaluations Work collaboratively...
Sr Clinical Research Associate
- Rosemont, IL (13 miles from Chicago, IL)
- 14 days ago
- Rosemont, IL (13 miles from Chicago, IL)
- 14 days ago
at Philips in Rosemont, Illinois, United States Job Description Senior Clinical Research Associate The Senior Clinical Research Associate ( CRA ) actively drives the execution of clinical trials in...
Job responsibilities * Performs site qualification, site initiation, interim monitoring, site management and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good...
Location: Chicago, Illinois Business Unit: Rush Medical Center Hospital: Rush University Medical Center Department: Pediatrics-Res Adm Work Type: Full Time (Total FTE between 0.9 and 1.0) Shift:...
.- Adhere to Good Clinical Practice (GCP) guidelines and all human subject protection practices Perform other duties as required.- Create systems for project implementation and data collection, including...
FSP Senior Clinical Research Associate - Psychiatry
- Western Springs, IL (14 miles from Chicago, IL)
- 18 days ago
- Western Springs, IL (14 miles from Chicago, IL)
- 18 days ago
Experience Requirements: 5 or more years of experience as a Clinical Research Associate....
Senior Clinical Site Manager (Sr. CRA), Texas
- Northbrook, IL (17 miles from Chicago, IL)
- 30+ days ago
- Northbrook, IL (17 miles from Chicago, 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...
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...
- Oak Forest, IL (21 miles from Chicago, IL)
- 30+ days ago
- Oak Forest, IL (21 miles from Chicago, IL)
- 30+ days ago
Commensurate with experience Responsibilities A CRA is responsible for performing procedures and coordinating the execution of clinical trials in accordance with research protocols....
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
- Federal Housing Administration
- Mortgage Lending
- FHLMC
- Federal National Morgage Association
- Nationwide Mortgage Licensing System & Registry
- Fannie Mae
- Institutional Review Board
- ICH GCP
- Clinical Trial Management System
- Sample Preparation
- Study Management
- Clinical Monitoring
- Clinical Data Management
- Gene Therapy
- ICH Guidelines
- Good Clinical Practice
- Medical Affairs
- Drug Development
- Pharmacovigilance
- Site Management
- Physiology
- Biotechnology
- Clinical Trials
- Clinical Research
- Neuroscience
- Clinical Operations
- Oncology
- Medical Device Sales
- FDA Regulations
- Data Collection
- Patient Care
- Standard Operating Procedures
- Data Management
- Collections
- Military Background
- High School Diploma
- Investigation
- Written Communication
- Auditing
- Presentation
- Documentation
- Collaboration
- Bachelor's Degree
- Reporting
- Education Experience
- Regulations
- Sales
- Policy Development
- Problem Solving
- Research Skills
- Microsoft Office
- Microsoft Excel
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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