Clinical Research Associate Jobs in Irvine, CA
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, Clinical Monitoring (Remote)
- Irvine, CA
- 8 days ago
- Irvine, CA
- 8 days ago
Research Associate Qualifications A minimum of 5 years' experience as a clinical research associate preferred with onsite monitoring and site management activities Knowledge and experience monitoring...
Research Associate Qualifications A minimum of 5 years experience as a clinical research associate preferred with onsite monitoring and site management activities Knowledge and experience monitoring...
Responsibilities The Clinical Research Associate (Coronary) role is a key position within the coronary program to help ensure FDA clearance through a PMA approval of this innovative device is granted...
Remote WorkUphold Good Clinical Practices, FDA Rules, NIH guidelines, HIPAA regulations, ICH guidelines, and institutional policies for clinical trials....
Uphold Good Clinical Practices, FDA Rules, NIH guidelines, HIPAA regulations, ICH guidelines, and institutional policies for clinical trials....
Clinical Research Associate II City of Hope Irvine, CA Full Time Published on 05/25/2025...
Position Objective: To independently manage and monitor all aspects of clinical trials at investigative sites, ensuring data accuracy and compliance with protocols, ICH-GCP guidelines, and applicable...
Clinical Study Coordinator Hybrid - Onsite in Irvine, CA every Tuesday, Thursday, and every other Friday Job Description: This professional will report to Clinical Science and External Research...
Clinical Study Coordinator Hybrid - Onsite every Tuesday, Thursday and every other Friday in Irvine, CA Job Description: This professional will report to Clinical Science and External Research...
Duarte Medical Center seeks a full-time, on-site Clinical Study Coordinator to support oncology clinical trials....
Demographic Data for Irvine, CA
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Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in Irvine, CA
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in Irvine, CA 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
- Fannie Mae
- Sample Preparation
- ICH GCP
- Institutional Review Board
- Study Management
- Clinical Monitoring
- Clinical Trial Management System
- Cancer Research
- Clinical Data Management
- Gene Therapy
- Good Clinical Practice
- ICH Guidelines
- Medical Affairs
- Biology
- Drug Development
- Site Management
- Biotechnology
- 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
- Documentation
- Interpersonal Skills
- Collaboration
- Reporting
- Data Entry
- Policy Development
- Bachelor's Degree
- Microsoft PowerPoint
- Regulations
- Microsoft Office
- Problem Solving
- Research Skills
- Microsoft Excel
- Teamwork
- Time Management
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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