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 • Conduct on-site and remote clinical monitoring visits to ensure compliance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements. • Manage a portfolio of approximately 2–3 clinical study protocols and 8–10 investigative sites. • Perform all types of monitoring visits, including site initiation, interim monitoring, and closeout visits. • Monitor site performance, review study documentation, and ensure accurate and complete clinical trial data. • Identify, document, and support the resolution of protocol deviations, compliance concerns, and site-level issues. • Collaborate with clinical operations teams and investigative site personnel to support study timelines and quality objectives. • Travel approximately 50% of the time, averaging 6–8 monitoring visits per month. Required Qualifications • Bachelor’s degree or equivalent four-year degree required. • Minimum of 2 years of clinical research monitoring experience as a CRA. • Experience supporting General Medicine clinical trials preferred. • Demonstrated experience conducting all types of clinical monitoring visits. • Ability to independently manage multiple protocols and a portfolio of approximately 8–10 sites. • Strong knowledge of GCP, clinical trial regulations, monitoring practices, and clinical documentation. • Willingness and ability to travel approximately 50% of the time. Additional Details • Sites will generally be assigned within the CRA’s home state or within a short, direct flight; neighboring states may be included. • Monitoring will be a combination of on-site and remote visits. • No on-site productivity metrics. • Collaborative team environment with a strong emphasis on employee retention and support. Interested in learning more? Apply today to explore this opportunity with a supportive clinical operations team. This job opens for applications on 10/17/2026. Applications for this job will be accepted for at least 30 days from the posting date. #LI-KP1 #LI-ONSITE