Clinical Research Associate (CRA) - A
Experis
Date: 1 day ago
City: Sunnyvale, CA
Salary:
$45
-
$50
per hour
Contract type: Contractor
Title: Clinical Research Associate (CRA)
Location: Sunnyvale, CA
Duration: 12 Months
Pay Range: $45 to $50/hr
We are looking for an Internal Clinical Research Associate (CRA) to join one of our growing Clinical Operations teams.
Job Summary
The Internal CRA will assist in managing clinical research sites throughout the entire trial lifecycle—from start-up to close-out—under the supervision of the Clinical Manager. The role involves conducting qualification, initiation, monitoring, and close-out visits, ensuring compliance with study protocols, SOPs, and GCP regulations.
Key Responsibilities
If you’re interested, please click the “Apply” button.
Location: Sunnyvale, CA
Duration: 12 Months
Pay Range: $45 to $50/hr
We are looking for an Internal Clinical Research Associate (CRA) to join one of our growing Clinical Operations teams.
Job Summary
The Internal CRA will assist in managing clinical research sites throughout the entire trial lifecycle—from start-up to close-out—under the supervision of the Clinical Manager. The role involves conducting qualification, initiation, monitoring, and close-out visits, ensuring compliance with study protocols, SOPs, and GCP regulations.
Key Responsibilities
- Manage clinical research sites through start-up, monitoring, and close-out phases.
- Conduct site qualification, initiation, monitoring, and close-out visits.
- Verify investigator qualifications, site facilities, and study documentation.
- Perform source data verification and ensure good documentation practices.
- Manage investigational product (IP) accountability and inventory.
- Review and ensure accurate reporting of adverse events.
- Support subject enrolment, recruitment, and retention efforts.
- Prepare monitoring reports and follow-up communications.
- Bachelor’s degree in Life Sciences, Clinical Research, or a related field required.
- Minimum 1 year of clinical research experience required.
- Experience with monitoring visits and regulatory compliance preferred.
- More than 2 years of experience, they are overqualified for this role
If you’re interested, please click the “Apply” button.
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