Clinical Research Associate Jobs in San Rafael, 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.
- Alameda, CA (18 miles from San Rafael, CA)
- 2 hours ago
- Alameda, CA (18 miles from San Rafael, CA)
- 2 hours ago
Assist and conduct clinical monitoring and site management activities, ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations, department procedures...
Clinical Research Associate I/CPT - MIRIAD IBD Biobank & Database
- Berkeley, CA (14 miles from San Rafael, CA)
- 11 days ago
- Berkeley, CA (14 miles from San Rafael, CA)
- 11 days ago
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
CRA III (Associate Clinical Research III)
- Alameda, CA (18 miles from San Rafael, CA)
- 15 days ago
- Alameda, CA (18 miles from San Rafael, CA)
- 15 days ago
Manage clinical monitoring activities and overall site management ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations, department procedures...
Associate Clinical Research III
- Alameda, CA (18 miles from San Rafael, CA)
- 16 days ago
- Alameda, CA (18 miles from San Rafael, CA)
- 16 days ago
Perform study site visits (SQV, SIV, IMV, COV), ensuring compliance with the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations, department procedures and applicable...
Clinical Trial Associate - Life Sciences
- South San Francisco, CA (22 miles from San Rafael, CA)
- 24 days ago
- South San Francisco, CA (22 miles from San Rafael, CA)
- 24 days ago
We are seeking a Life Sciences-Clinical Trial Associate for an assignment in South San Francisco California....
- Alameda, CA (18 miles from San Rafael, CA)
- 27 days ago
- Alameda, CA (18 miles from San Rafael, CA)
- 27 days ago
Strong understanding of regulatory compliance, Good Clinical Practices (GCP), and clinical study protocols....
Senior Clinical Trial Associate
- South San Francisco, CA (22 miles from San Rafael, CA)
- 28 days ago
- South San Francisco, CA (22 miles from San Rafael, CA)
- 28 days ago
Responsibilities Adhere to Clinical Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and International Conference on Harmonization (ICH) Guidelines....
- Alameda, CA (18 miles from San Rafael, CA)
- 29 days ago
- Alameda, CA (18 miles from San Rafael, CA)
- 29 days ago
Ensure adherence to Good Clinical Practices, Industry standards, standard operating procedures and to all other regulatory and quality standards in conducting our organization Clinical research and...
CRA I (Associate I Clinical Research)
- Alameda, CA (18 miles from San Rafael, CA)
- 30+ days ago
- Alameda, CA (18 miles from San Rafael, CA)
- 30+ days ago
Assist and conduct clinical monitoring and site management activities, ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations, department procedures...
- Alameda, CA (18 miles from San Rafael, CA)
- 30+ days ago
- Alameda, CA (18 miles from San Rafael, CA)
- 30+ days ago
Assist and conduct clinical monitoring and site management activities, ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations, department procedures...
Clinical Trials Research Coordinator
- San Francisco, CA (14 miles from San Rafael, CA)
- 30+ days ago
- San Francisco, CA (14 miles from San Rafael, CA)
- 30+ days ago
This is a non-licensed position which works under the daily supervision of an experienced Clinical Trial Nurse, Clinical Trial Research Coordinator, and/or KFRI-designated, licensed clinical trial research...
Senior Clinical Research Monitor
- San Francisco, CA (14 miles from San Rafael, CA)
- 60+ days ago
- San Francisco, CA (14 miles from San Rafael, CA)
- 60+ days ago
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...
Demographic Data for San Rafael, CA
Moving to San Rafael, CA? Find some basic demographic data about San Rafael, CA below.
Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in San Rafael, CA
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in San Rafael, CA offer the following education backgroundQualifications / Skill Sets
The following top skills are often required or desired to land a Clinical Research Associate position
- Mortgage Lending
- FHLMC
- Fannie Mae
- Sample Preparation
- Institutional Review Board
- ICH GCP
- Study Management
- Clinical Monitoring
- Clinical Trial Management System
- Clinical Data Management
- Gene Therapy
- Good Clinical Practice
- ICH Guidelines
- Specimen Processing
- Biology
- Drug Development
- Pharmacovigilance
- Site Management
- Biotechnology
- Physiology
- 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
- Interpersonal Skills
- Quality Assurance
- Collaboration
- Documentation
- Reporting
- Data Entry
- Bachelor's Degree
- Regulations
- Policy Development
- Microsoft Office
- Problem Solving
- Research Skills
- Microsoft Excel
- Time Management
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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