Eastridge Workforce Solutions partners with leading life sciences organizations to connect skilled clinical research professionals with work that truly makes an impact. We’re supporting a high growth client in need of a Clinical Research Associate who’s excited to play a key role in advancing global studies and strengthening site relationships.
Job Title: Clinical Research Associate
Location: Remote
Pay Range: $55 - $68/hr DOE
Employment Type: Temporary
This is a great opportunity for a CRA who enjoys both autonomy and collaboration, wants meaningful visibility across multiple study phases, and thrives in environments where quality, readiness, and strong site engagement matter. You’ll support domestic and international trials, work closely with a knowledgeable clinical operations team, and contribute directly to the success of high priority studies.
What You’ll Do
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Lead site qualification, initiation, monitoring, and close-out visits, ensuring sites are set up for success and consistently meeting protocol requirements.
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Partner closely with Senior CRAs to build clean, intuitive source documentation and case report forms aligned to protocol needs.
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Guide sites through informed consent requirements, create site specific language, and support IRB submissions to keep timelines moving.
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Train coordinators and site staff so they feel confident in data capture, documentation, and study expectations.
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Monitor data quality and safety reporting, confirm source accuracy, and proactively address deviations or issues.
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Maintain a real time, inspection ready Trial Master File and ensure critical documents are always up to date.
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Contribute to clinical study report development, data validation activities, and other critical study deliverables.
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Join team meetings, capture and track action items, and help keep cross functional communication aligned.
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Support overall compliance with SOPs, ICH GCP, and local/global regulations.
What You Bring
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BA or BS degree, or equivalent combination of education and relevant experience.
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Three or more years of experience monitoring or supporting the execution of clinical trials.
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Comfort traveling up to 60 percent and managing travel independently.
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Strong analytical skills, high attention to detail, and the ability to build positive, solution oriented site relationships.
Benefits: Use this link bit.ly/4cGUQSh to learn more about benefits available to Eastridge’s temporary employees. From time to time Eastridge’s clients may offer additional benefits to Eastridge employees while on assignment. Information about those benefits will be communicated when applicable.
Eastridge Workforce Solutions is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. We celebrate diversity and are committed to creating an inclusive environment for all employees. Please note that Eastridge is unable to provide visa sponsorship to applicants.
Certain clients require Eastridge to perform background checks and Eastridge will consider qualified applicants with criminal histories in a manner consistent with any applicable federal, state, or local law regarding criminal backgrounds, including but not limited to the Los Angeles Fair Chance Initiative for Hiring and the San Francisco Fair Chance Ordinance.
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