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.
, this position Serves as a Clinical Research Specialist within the Clinical R&D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and...
HybridJoin a Team That's Advancing Clinical Research We're looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical trials...
In PersonJoin a Team That's Advancing Clinical Research We're looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical trials...
In Person- Bayside Solutions
- Redwood City, CA
- 2 days ago
- Redwood City, CA
- 2 days ago
Clinical Research Associate in Redwood City, California Overview Sr. Clinical Research Associate W2 Contract Pay Rate: $75 - $85 per hour Location: Redwood City, CA - Hybrid Role Job Summary: Sr....
Hybrid- Biolinq Incorporated
- San Diego, CA
- 2 days ago
- San Diego, CA
- 2 days ago
Clinical Practice guidelines and regulations for conducting human clinical studies Knowledge of the Health Insurance Portability and Accountability Act (HIPAA) and the ability to manage Protected Health...
In PersonClinical Research Associate I - Spine Research - Department of Neurosurgery
- Cedars-Sinai
- 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....
In PersonTemporary Clinical Research Assistant
- University of California System
- Orange, CA
- 4 days ago
- Orange, CA
- 4 days ago
Preferred: Prior experience supporting clinical trials or research study coordination activities. Familiarity with Clinical Trial Management Systems such as OnCore or similar research platforms....
In Person TemporarySenior Clinical Research Associate
- Travere Therapeutics
- San Diego, CA
- 4 days ago
- San Diego, CA
- 4 days ago
Demonstrates working knowledge in global regulatory and compliance requirements for clinical research, including but not limited to US CFR, EU CTD, and ICH GCP....
In PersonClinical Research Associate II
- Corcept Therapeutics
- Redwood City, CA
- 4 days ago
- Redwood City, CA
- 4 days ago
The Clinical Research Associate (CRA) II monitors clinical study activities to assure adherence to Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs), and study protocols....
In PersonInternal Clinical Research Associate (East Coast Remote)
- Cordis
- Irvine, CA
- 5 days ago
- Irvine, CA
- 5 days ago
protocols, Good Clinical Practice (GCP), and applicable regulatory requirements....
RemotePreferred: Prior experience supporting clinical trials or research study coordination activities. Familiarity with Clinical Trial Management Systems such as OnCore or similar research platforms....
In Person TemporaryClinical Research Associate I - Regenerative Medicine Institute
- Cedars-Sinai
- Los Angeles, CA
- 5 days ago
- Los Angeles, CA
- 5 days ago
Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines...
In PersonClinical Research Associate - Multi Therapeutic Area (Early Development) - West Region ICON plc is a world-leading healthcare intelligence and clinical research organization....
In PersonClinical Trial Associate (Hybrid - Acton, MA)
- Insulet Corporation
- San Diego, CA
- 7 days ago
- San Diego, CA
- 7 days ago
Provide functional guidance to Clinical Trial Coordinators or Clinical Trial Associates on projectrelated deliverables, as appropriate....
HybridClinical Research Associate II- Shockwave
- Johnson & Johnson
- Santa Clara, CA
- 7 days ago
- Santa Clara, CA
- 7 days ago
Position Overview The Clinical Research Associate II (CRA II) is responsible for facilitating in-house set up, activation, maintenance and closure of global clinical trials while gaining experience...
RemoteDemographic 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
- Fannie Mae
- Good Clinical Practice
- ICH Guidelines
- Study Management
- Sample Preparation
- Institutional Review Board
- Clinical Monitoring
- ICH GCP
- Clinical Trial Management System
- Drug Development
- Biostatistics
- Gene Therapy
- Pharmacovigilance
- Cancer Research
- Biology
- Site Management
- Clinical Trials
- Clinical Operations
- Clinical Research
- Biotechnology
- Neuroscience
- Medical Device Sales
- FDA Regulations
- Oncology
- Data Collection
- Standard Operating Procedures
- Data Management
- Health Care
- Collections
- Auditing
- Investigation
- Documentation
- Implementation
- Verbal Communication
- Reporting
- Policy Development
- Data Entry
- Collaboration
- Education Experience
- Microsoft PowerPoint
- Bachelor's Degree
- Microsoft Word
- Regulations
- Research Skills
- Microsoft Excel
- Microsoft Office
- Problem Solving
- Staff Supervision
- Scheduling
- Computer Skills
- Time Management
- Leadership
- Communication Skills
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