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.
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
Clinical Research Associate I - Biomedical Imaging Research Institute
- Beverly Hills, CA
- 1 day ago
- Beverly Hills, CA
- 1 day 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
- 30+ days ago
- Los Angeles, CA
- 30+ 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 -Heart Institute
- 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....
Clinical Research Associate I - Karsh Division of Gastroenterology and Hepatology (Per Diem)
- Los Angeles, CA
- 30+ days ago
- Los Angeles, CA
- 30+ 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
- 30+ days ago
- Los Angeles, CA
- 30+ 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
- 30+ days ago
- Los Angeles, CA
- 30+ 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 Specialist I - Gastroenterology and Hepatology Division/Department of Medicine
- 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....
Schwab is looking for a motivated Clinical Research Associate I to join his team!...
Senior Clinical Research Associate (West Coast) Remote Position
- Bakersfield, CA
- 23 hours ago
- Bakersfield, CA
- 23 hours ago
This is what you will do: The Senior Clinical Research Associate (Sr....
Oversight/execution of feasibility, selection, set up, conduct and closure of a clinical trial within the allocated countries, in accordance with the ICH-GCP, applicable legislation and Company Standard...
Principal Clinical Research Associate - Shockwave Medical (Remote)
- Santa Clara, CA
- 2 days ago
- Santa Clara, CA
- 2 days ago
Principal Clinical Research Associate - Shockwave Medical (Remote)- Function R D Operations- Sub function Clinical Trial Project Management- Category Senior Analyst, Clinical Trial Project Management...
Remote WorkDescription:** The SCRA is primarily a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP...
., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines....
Senior Clinical Site Manager (Sr. CRA), California
- Los Angeles, CA
- 4 days ago
- Los Angeles, CA
- 4 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...
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
- Consumer Lending
- Mortgage Lending
- FHLMC
- Federal National Morgage Association
- Nationwide Mortgage Licensing System & Registry
- Fannie Mae
- Institutional Review Board
- ICH GCP
- Sample Preparation
- Clinical Trial Management System
- Study Management
- Clinical Monitoring
- Clinical Data Management
- Good Clinical Practice
- Gene Therapy
- ICH Guidelines
- Cancer Research
- Drug Development
- Scientific Research
- Site Management
- Pharmacovigilance
- Biotechnology
- Clinical Trials
- Neuroscience
- Clinical Research
- Clinical Operations
- Oncology
- FDA Regulations
- Medical Device Sales
- Data Collection
- Patient Care
- Standard Operating Procedures
- Data Management
- Affirmative Action
- Collections
- High School Diploma
- Investigation
- Written Communication
- Auditing
- Documentation
- Data Entry
- Collaboration
- Reporting
- Education Experience
- Microsoft PowerPoint
- Regulations
- Policy Development
- Problem Solving
- Microsoft Office
- Microsoft Excel
- Teamwork
- Staff Supervision
- Organization
- Research Skills
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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