Clinical Research Associate Jobs in Alameda, 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.
Clinical Research Associate I/CPT - MIRIAD IBD Biobank & Database
- Berkeley, CA (6 miles from Alameda, CA)
- 11 hours ago
- Berkeley, CA (6 miles from Alameda, CA)
- 11 hours ago
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board....
- Palo Alto, CA (23 miles from Alameda, CA)
- 1 day ago
- Palo Alto, CA (23 miles from Alameda, CA)
- 1 day ago
Tekberry is looking for a highly qualified and motivated Clinical Research Associate to work on-site with our client, a world-class university and research center....
Clinical Research Assistant Nuclear Medicine Service
- Palo Alto, CA (23 miles from Alameda, CA)
- 1 day ago
- Palo Alto, CA (23 miles from Alameda, CA)
- 1 day ago
trials Good Clinical Practice Oncology Communication skills FDA regulations Under 1 year Full Job Description Palo Alto Veterans Institute for Research (PAVIR) is seeking a full-time Clinical Research...
Clinical Research Assistant Nuclear Medicine Service PAVIR
- Palo Alto, CA (23 miles from Alameda, CA)
- 2 days ago
- Palo Alto, CA (23 miles from Alameda, CA)
- 2 days ago
; Ability to effectively present information and respond to questions from sponsor/CRO, physicians, staff and patients is desired; Knowledge of following: Principles of Good Clinical Practice (GCP),...
Manage clinical monitoring activities and overall site management ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal Regulations, department procedures...
- Palo Alto, CA (23 miles from Alameda, CA)
- 5 days ago
- Palo Alto, CA (23 miles from Alameda, CA)
- 5 days ago
Our client, [Industry Descriptor] is seeking a [Job Title] to join their team. As a [Job Title], you will be part of the [Department Name] supporting [Team Name(s)]. The ideal candidate will have...
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...
- Palo Alto, CA (23 miles from Alameda, CA)
- 5 days ago
- Palo Alto, CA (23 miles from Alameda, CA)
- 5 days ago
Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred....
Senior Clinical Research Associate
- Menlo Park, CA (22 miles from Alameda, CA)
- 7 days ago
- Menlo Park, CA (22 miles from Alameda, CA)
- 7 days ago
We are proactively identifying candidates for a potential part-time Clinical Research Associate (CRA) position supporting global Phase II/III oncology trials....
Senior Clinical Research Associate
- Foster City, CA (15 miles from Alameda, CA)
- 9 days ago
- Foster City, CA (15 miles from Alameda, CA)
- 9 days ago
Knowledge, Skills and Abilities: Good knowledge of ICH GCP and FDA/EMA regulations Good verbal and strong written communication skills. Highly organized and detail oriented....
Clinical Trial Associate - Life Sciences
- South San Francisco, CA (11 miles from Alameda, CA)
- 13 days ago
- South San Francisco, CA (11 miles from Alameda, CA)
- 13 days ago
We are seeking a Life Sciences-Clinical Trial Associate for an assignment in South San Francisco California....
Strong understanding of regulatory compliance, Good Clinical Practices (GCP), and clinical study protocols....
Senior Clinical Trial Associate
- South San Francisco, CA (11 miles from Alameda, CA)
- 17 days ago
- South San Francisco, CA (11 miles from Alameda, CA)
- 17 days ago
Responsibilities Adhere to Clinical Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and International Conference on Harmonization (ICH) Guidelines....
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...
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...
Demographic Data for Alameda, CA
Moving to Alameda, CA? Find some basic demographic data about Alameda, CA below.
Clinical Research Associate Online Courses and Training Opportunities
Salary for Clinical Research Associate Jobs in Alameda, CA
Required or preferred licenses and certifications for Clinical Research Associate positions.
Highest Education Level
Clinical Research Associates in Alameda, 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
- Nationwide Mortgage Licensing System & Registry
- Fannie Mae
- Sample Preparation
- Institutional Review Board
- ICH GCP
- Study Management
- Clinical Monitoring
- Clinical Trial Management System
- Gene Therapy
- ICH Guidelines
- Good Clinical Practice
- Drug Development
- Biology
- Centrifuge
- DNA Isolation
- Site Management
- Biotechnology
- Physiology
- Clinical Trials
- Clinical Research
- Neuroscience
- Clinical Operations
- Oncology
- Medical Device Sales
- FDA Regulations
- Data Collection
- Standard Operating Procedures
- Patient Care
- Data Management
- Health Care
- Collections
- Auditing
- Investigation
- Written Communication
- Collaboration
- Documentation
- Education Experience
- Bachelor's Degree
- Data Entry
- Reporting
- Microsoft PowerPoint
- Regulations
- Inventory Management
- 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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