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Clinical research associate • fontana ca
- Promoted
Clinical Research Associate (CRA)
Piper CompaniesCalifornia, CA- Promoted
California Licensed Clinical Research Associate
VirtualVocationsFontana, California, United States- Promoted
Sr. Clinical Research Coordinator
Universal Healthcare ResourcesRiverside, CA, United StatesClinical Research Coordinator
IQVIAColton, CA, US- Promoted
Clinical Trial Associate
Bayside SolutionsSan Mateo County, CA, United StatesSenior Clinical Research Associate - Oncology - West Coast
Worldwide Clinical TrialsCalifornia, USA- Promoted
Principal Investigator in Clinical Research (Neurology, Psychiatry)
Site Search RecruitmentRiverside, CA, United StatesManager-Clinical Research
Loma Linda Unv Shared ServicesSan Bernardino, California- Promoted
Job Title : Sr. Clinical Research Coordinator
ComriseRiverside, CA, United States- Promoted
Sr. / Research Associate, Assay Development
Hydrogen GroupSan Mateo County, CA, United StatesResearch Associate
R&D PartnersCalifornia, CAClinical Research Coordinator II (Oncology)
Children’s Hospital of Orange CountyCA, USClinical Research Associate I - Biomedical Imaging Research Institute
Cedars-SinaiCA, United StatesClinical Research Assistant
ActalentRiverside, California, USA- Promoted
Sub-Investigator (NP or PA)
Irvine Clinical ResearchRiverside, CA, United StatesBH Associate Provider - Associate Clinical Social Worker
Careerbuilder-USFontana, CA, United StatesClinical Research Pharmacy Services Manager
ICONMARemote, CA- Promoted
Travel Clinical Research Coordinator - $1,961 per week
PRIDE HealthTextile Finance, CA, United StatesClinical Research Associate (CRA)
Piper CompaniesCalifornia, CA- Full-time
Piper Companies is seeking an experienced Clinical Research Associate (CRA) to join our client’s team. This opportunity is with an industry-leading Clinical Research organization supporting one of the top pharmaceutical companies in the world. The CRA will play a critical role in monitoring and managing clinical trials, ensuring compliance with regulatory requirements, and maintaining high standards of data integrity and patient safety.
Locations for the Clinical Research Associate : United States (PST, MST, CST) and Canada
Responsibilities for the Clinical Research Associate :
- Monitor clinical trials to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
- Conduct site visits, including pre-study, initiation, monitoring, and close-out visits.
- Review and verify case report forms (CRFs) and source documents for accuracy and completeness.
- Ensure timely and accurate reporting of adverse events and protocol deviations.
- Provide training and support to site staff on study protocols, procedures, and regulatory requirements.
- Maintain effective communication with study sites, investigators, and other stakeholders.
- Assist in the preparation and review of study-related documentation, including informed consent forms, study manuals, and monitoring plans.
- Participate in study team meetings and provide updates on site status and study progress.
Qualifications for the Clinical Research Associate :
Compensation / Benefits for the Clinical Research Associate :
This job opens for applications on 4 / 17 / 2025. Applications for this job will be accepted for at least 30 days from the posting date.
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