Clinical Research Associate Jobs in San Diego, 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.
**You're the right fit if:** + You've acquired 2+ years of experience as a Clinical Research Associate (CRA), ideally within the medical device industry, including experience managing clinical trials...
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...
Conducts Site Qualification, Initiation, Interim Monitoring, Close-Out visits and activities independently and in accordance with FDA Code of Federal Regulations, Good Clinical Practice, guidelines,...
Experience with using electronic data capture systems (EDC), Clinical Trial Management Systems (CTMS), and electronic trial master files (eTMF)....
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Senior Clinical Site Manager (Sr. CRA), California
- San Diego, CA
- 17 days ago
- San Diego, CA
- 17 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...
Coordinate multiple aspects of clinical trials and other human research ensuring compliance with research protocol and IRB requirements....
trial practices and regulations Working knowledge of clinical trial databases Proficient computer skills including Microsoft Office Suite Required Qualifications Minimum BA or BS and 2 years of related...
Clinical Practice (ICH-GCP)....
Clinical Site Manager, Physical Rehabilitation Services
- San Diego, CA
- 90+ days ago
- San Diego, CA
- 90+ days ago
Impact Lives, Impact Community Family Health Centers of San Diego (FHCSD) is passionate about providing exceptional health care to all, especially underserved communities with limited health care...
Demographic Data for San Diego, CA
Moving to San Diego, CA? Find some basic demographic data about San Diego, CA below.
Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in San Diego, CA
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in San Diego, 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
- 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
- Gene Therapy
- ICH Guidelines
- Good Clinical Practice
- Medical Affairs
- Drug Development
- Pharmacovigilance
- Site Management
- Physiology
- Clinical Trials
- Biotechnology
- Clinical Research
- Clinical Operations
- Anatomy and Physiology
- Oncology
- Medical Device Sales
- FDA Regulations
- Data Collection
- Patient Care
- Standard Operating Procedures
- Data Management
- Collections
- Military Background
- Investigation
- Written Communication
- Auditing
- Presentation
- Documentation
- Collaboration
- Bachelor's Degree
- Reporting
- Education Experience
- Regulations
- Sales
- Policy Development
- Problem Solving
- Research Skills
- Microsoft Office
- Microsoft Excel
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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