Clinical Research Associate Jobs in California
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 I, PER_DIEM -Heart Institute
- Los Angeles, CA
- 4 days ago
- Los Angeles, CA
- 4 days ago
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
Clinical Research Associate I, PER DIEM - Tan Lab
- Sacramento, CA
- 8 days ago
- Sacramento, CA
- 8 days ago
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
Clinical Research Associate I -Heart Institute, Cheng Lab
- Los Angeles, CA
- 8 days ago
- Los Angeles, CA
- 8 days ago
Assists with regulatory submissions to the Institutional Review Board (IRB) and works closely with supervising research staff or directly with the Institutional Review Board to submit Adverse Events...
Clinical Research Associate I - Karsh Division of Gastroenterology and Hepatology (Per Diem)
- Los Angeles, CA
- 8 days ago
- Los Angeles, CA
- 8 days ago
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
Clinical Research Associate I (Per Diem) - Smidt Heart Institute
- Los Angeles, CA
- 8 days ago
- Los Angeles, CA
- 8 days ago
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
Clinical Research Associate I - Heart Institute
- Los Angeles, CA
- 8 days ago
- Los Angeles, CA
- 8 days ago
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
Clinical Research Associate I - Berman Lab Cedars-Sinai Medical Center
- Los Angeles, CA
- 1 day ago
- Los Angeles, CA
- 1 day ago
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
Alameda : 1360-1380 South Loop Road ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Yes, 10 % of the Time MEDICAL SURVEILLANCE: Not Applicable SIGNIFICANT WORK ACTIVITIES: Continuous sitting...
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...
Responsibilities include patient recruitment, informed consent, trial coordination, data management, and regulatory compliance....
What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards....
Remote WorkClinical Research Associate I - Per diem, Schwab Lab
- California City, CA
- 2 days ago
- California City, CA
- 2 days ago
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board. ?...
Strong knowledge of GCP, ICH guidelines, and regulatory requirements. Experience in site management, patient recruitment, and clinical trial documentation....
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
Clinical Research Associate I, PER_DIEM -Heart Institute Cedars-Sinai Medical Center
- Los Angeles, CA
- 4 days ago
- Los Angeles, CA
- 4 days ago
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
Demographic Data for California
Moving to California? Find some basic demographic data about California below.
Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in California
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in California 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
- Fannie Mae
- ICH GCP
- Institutional Review Board
- Sample Preparation
- Clinical Trial Management System
- Study Management
- Clinical Monitoring
- Clinical Data Management
- Gene Therapy
- ICH Guidelines
- Good Clinical Practice
- Cancer Research
- Drug Development
- Scientific Research
- Site Management
- Physiology
- Biotechnology
- Neuroscience
- Clinical Trials
- Clinical Operations
- Clinical Research
- Anatomy and Physiology
- Oncology
- FDA Regulations
- Medical Device Sales
- Data Collection
- Patient Care
- Standard Operating Procedures
- Data Management
- Phlebotomy
- Affirmative Action
- Collections
- Investigation
- Auditing
- Presentation
- Written Communication
- Documentation
- Quality Assurance
- Collaboration
- Data Entry
- Bachelor's Degree
- Reporting
- Education Experience
- Regulations
- Policy Development
- Research Skills
- Microsoft Office
- Microsoft Excel
- Problem Solving
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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