Clinical Research Associate Jobs in Kansas City, KS
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.
Clinical Research Associate, Sponsor Dedicated
- Overland Park, KS (21 miles from Kansas City, KS)
- 3 days ago
- Overland Park, KS (21 miles from Kansas City, KS)
- 3 days ago
Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines....
Clinical Research Associate, Full Service
- Overland Park, KS (21 miles from Kansas City, KS)
- 4 days ago
- Overland Park, KS (21 miles from Kansas City, KS)
- 4 days ago
As you develop your career as a CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA, we do not believe in a career ceiling. You can...
Clinical Research Assistant - Internal Medicine (Pulmonary) - JR008711
- Kansas City, KS
- 4 days ago
- Kansas City, KS
- 4 days ago
trials by assisting with various aspects of research, including participant recruitment, data collection, and compliance with regulatory guidelines....
Clinical Research Assistant - Internal Medicine (Pulmonary)
- Kansas City, MO (1 mile from Kansas City, KS)
- 10 days ago
- Kansas City, MO (1 mile from Kansas City, KS)
- 10 days ago
trials by assisting with various aspects of research, including participant recruitment, data collection, and compliance with regulatory guidelines....
Clinical Research Assistant - Internal Medicine (Pulmonary)
- Kansas City, KS
- 12 days ago
- Kansas City, KS
- 12 days ago
trials by assisting with various aspects of research, including participant recruitment, data collection, and compliance with regulatory guidelines....
Senior CRA - Oncology Early Phase - Kansas City, Nebraska or St. Louis
- Kansas City, MO (1 mile from Kansas City, KS)
- 45+ days ago
- Kansas City, MO (1 mile from Kansas City, KS)
- 45+ days ago
Trials may include both early and late phase clinical trials. Develops meaningful site relationships through consistent collaborative communication and engagement....
Sr. CRA, Sponsor Aligned, Oncology
- Overland Park, KS (21 miles from Kansas City, KS)
- 45+ days ago
- Overland Park, KS (21 miles from Kansas City, KS)
- 45+ days ago
Job Overview: Join our dynamic team as a Clinical Research Associate!...
Demographic Data for Kansas City, KS
Moving to Kansas City, KS? Find some basic demographic data about Kansas City, KS below.
Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in Kansas City, KS
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in Kansas City, KS offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Research Associate position
- Mortgage Lending
- FHLMC
- Nationwide Mortgage Licensing System & Registry
- Fannie Mae
- Sample Preparation
- Institutional Review Board
- ICH GCP
- Study Management
- Clinical Monitoring
- Clinical Trial Management System
- Gene Therapy
- ICH Guidelines
- Good Clinical Practice
- Drug Development
- Biology
- Centrifuge
- DNA Isolation
- Site Management
- Biotechnology
- Physiology
- Clinical Trials
- Clinical Research
- Neuroscience
- Clinical Operations
- Oncology
- Medical Device Sales
- FDA Regulations
- Data Collection
- Standard Operating Procedures
- Patient Care
- Data Management
- Health Care
- Collections
- Auditing
- Investigation
- Written Communication
- Collaboration
- Documentation
- Education Experience
- Bachelor's Degree
- Data Entry
- Reporting
- Microsoft PowerPoint
- Regulations
- Inventory Management
- Policy Development
- Microsoft Office
- Problem Solving
- Research Skills
- Microsoft Excel
- Time Management
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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