Clinical Research Associate Jobs in North Las Vegas, NV
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 - Oncology - West Region (Field-Based)
- Las Vegas, NV (2 miles from North Las Vegas, NV)
- 1 day ago
- Las Vegas, NV (2 miles from North Las Vegas, NV)
- 1 day ago
As a Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence....
Community Banking Manager - CRA and Fair Lending
- Las Vegas, NV (2 miles from North Las Vegas, NV)
- 2 days ago
- Las Vegas, NV (2 miles from North Las Vegas, NV)
- 2 days ago
The Community Banking Manager - CRA & Fair Lending Officer - 1st Line of Defense (1LOD) is responsible for integrating Community Reinvestment Act (CRA) and Fair Lending compliance into the daily...
Clinical Research Associate, Sponsor Dedicated
- Las Vegas, NV (2 miles from North Las Vegas, NV)
- 30+ days ago
- Las Vegas, NV (2 miles from North Las Vegas, NV)
- 30+ days ago
Req 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....
CRA 2 - Oncology, U.S. East Coast, Central or West Coast
- Las Vegas, NV (2 miles from North Las Vegas, NV)
- 30+ days ago
- Las Vegas, NV (2 miles from North Las Vegas, NV)
- 30+ days 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)....
- Las Vegas, NV (2 miles from North Las Vegas, NV)
- 60+ days ago
- Las Vegas, NV (2 miles from North Las Vegas, NV)
- 60+ days ago
Ensures the investigator’s adherence to the approved protocol and all Good Clinical Practice (GCP) procedures....
Senior Clinical Research Monitor
- Las Vegas, NV (2 miles from North Las Vegas, NV)
- 60+ days ago
- Las Vegas, NV (2 miles from North Las Vegas, NV)
- 60+ days ago
Determine if clinical trial/study subject documentation aligns with the study hypothesis and monitor clinical trial/study safety in accordance with protocols, Good Clinical Practices (GCP), and regulatory...
Demographic Data for North Las Vegas, NV
Moving to North Las Vegas, NV? Find some basic demographic data about North Las Vegas, NV below.
Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in North Las Vegas, NV
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in North Las Vegas, NV 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
- Fannie Mae
- Sample Preparation
- Institutional Review Board
- ICH GCP
- Study Management
- Clinical Monitoring
- Clinical Trial Management System
- Clinical Data Management
- Gene Therapy
- Good Clinical Practice
- ICH Guidelines
- Specimen Processing
- Biology
- Centrifuge
- Drug Development
- Site Management
- Biotechnology
- Physiology
- Clinical Trials
- Clinical Research
- Neuroscience
- Clinical Operations
- Oncology
- Medical Device Sales
- FDA Regulations
- Data Collection
- Patient Care
- Standard Operating Procedures
- Data Management
- Health Care
- Collections
- Auditing
- Investigation
- Written Communication
- Education Experience
- Quality Assurance
- Collaboration
- Documentation
- Reporting
- Bachelor's Degree
- Inventory Management
- Regulations
- Microsoft PowerPoint
- 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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