About this role
Clinical Research Associate II (CRA II)
Location: Florida, Georgia, or Texas (Central Florida preferred for Florida-based roles)
Compensation: Up to $115,000 annually; up to $118,000 for highly qualified candidates
Position Type: Full-Time
Travel: Approximately 50%
Target Start Date: November 9, 2026
About the Opportunity
We are seeking experienced Clinical Research Associate II (CRA II) professionals to support a leading biopharmaceutical organization’s clinical research programs. This is an excellent opportunity to join a collaborative, supportive clinical operations team focused on General Medicine studies.
The ideal candidate will have at least two years of clinical monitoring experience, a strong understanding of clinical trial site management, and experience conducting all types of monitoring visits. This role offers a hybrid monitoring model, a manageable site portfolio, and no on-site productivity metrics.
Key Responsibilities
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Conduct on-site and remote clinical monitoring visits to ensure compliance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements.
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Manage a portfolio of approximately 2–3 clinical study protocols and 8–10 investigative sites.
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Perform all types of monitoring visits, including site initiation, interim monitoring, and closeout visits.
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Monitor site performance, review study documentation, and ensure accurate and complete clinical trial data.
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Identify, document, and support the resolution of protocol deviations, compliance concerns, and site-level issues.
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Collaborate with clinical operations teams and investigative site personnel to support study timelines and quality objectives.
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Travel approximately 50% of the time, averaging 6–8 monitoring visits per month.
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Required Qualifications
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Bachelor’s degree or equivalent four-year degree required.
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Minimum of 2 years of clinical research monitoring experience as a CRA.
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Experience supporting General Medicine clinical trials preferred.
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Demonstrated experience conducting all types of clinical monitoring visits.
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Ability to independently manage multiple protocols and a portfolio of approximately 8–10 sites.
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Strong knowledge of GCP, clinical trial regulations, monitoring practices, and clinical documentation.
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Willingness and ability to travel approximately 50% of the time.
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Additional Details
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Sites will generally be assigned within the CRA’s home state or within a short, direct flight; neighboring states may be included.
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Monitoring will be a combination of on-site and remote visits.
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No on-site productivity metrics.
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Collaborative team environment with a strong emphasis on employee retention and support.
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Interested in learning more? Apply today to explore this opportunity with a supportive clinical operations team.
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This job opens for applications on 11/11/2026. Applications for this job will be accepted for at least 30 days from the posting date.