Clinical Research Associate Jobs in Concord, 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.
Senior Clinical Trial Associate
- San Francisco, CA (24 miles from Concord, CA)
- 2 days ago
- San Francisco, CA (24 miles from Concord, CA)
- 2 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 Concord, CA)
- 2 days ago
- Alameda, CA (18 miles from Concord, CA)
- 2 days ago
Solid understanding and demonstrated experience of the clinical trial process including study design and conduct; clinical data management systems; clinical trial management systems; data analysis;...
- Alameda, CA (18 miles from Concord, CA)
- 3 days ago
- Alameda, CA (18 miles from Concord, CA)
- 3 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 Research Associate I/CPT - MIRIAD IBD Biobank & Database
- Berkeley, CA (14 miles from Concord, CA)
- 15 days ago
- Berkeley, CA (14 miles from Concord, CA)
- 15 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 Concord, CA)
- 18 days ago
- Alameda, CA (18 miles from Concord, CA)
- 18 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 Concord, CA)
- 20 days ago
- Alameda, CA (18 miles from Concord, CA)
- 20 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...
- Alameda, CA (18 miles from Concord, CA)
- 30+ days ago
- Alameda, CA (18 miles from Concord, CA)
- 30+ days ago
Strong understanding of regulatory compliance, Good Clinical Practices (GCP), and clinical study protocols....
- Alameda, CA (18 miles from Concord, CA)
- 30+ days ago
- Alameda, CA (18 miles from Concord, CA)
- 30+ 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 Concord, CA)
- 30+ days ago
- Alameda, CA (18 miles from Concord, 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 Concord, CA)
- 30+ days ago
- Alameda, CA (18 miles from Concord, 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 (24 miles from Concord, CA)
- 45+ days ago
- San Francisco, CA (24 miles from Concord, CA)
- 45+ 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 (24 miles from Concord, CA)
- 60+ days ago
- San Francisco, CA (24 miles from Concord, 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 Concord, CA
Moving to Concord, CA? Find some basic demographic data about Concord, CA below.
Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in Concord, CA
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in Concord, 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
- Fannie Mae
- Sample Preparation
- ICH GCP
- Institutional Review Board
- Study Management
- Clinical Monitoring
- Clinical Trial Management System
- Clinical Data Management
- Gene Therapy
- Good Clinical Practice
- ICH Guidelines
- Biology
- Drug Development
- 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
- Technical Writing
- Health Care
- Collections
- Auditing
- Investigation
- Written Communication
- Presentation
- Education Experience
- Interpersonal Skills
- Collaboration
- Documentation
- Reporting
- Data Entry
- Policy Development
- Bachelor's Degree
- Regulations
- Microsoft Office
- Problem Solving
- Research Skills
- Microsoft Excel
- Staff Supervision
- Organization
- Scheduling
- Computer Skills
- Leadership
- Communication Skills
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