Clinical Research Assistant at Elite Clinical Network North Las Vegas, NV

Clinical Research Assistant job at Elite Clinical Network. North Las Vegas, NV.

We are seeking a highly motivated Clinical Research Assistant to support the day-to-day operations of ongoing clinical trials. This is an excellent opportunity to join a mission-driven team focused on advancing new therapies through rigorous and ethical clinical research. The ideal candidate will bring scientific curiosity, strong organizational skills, and a commitment to quality and compliance.

In this role you will be responsible for scheduling and rescheduling appointments, patient recruitment (including managing incoming calls),
printing source visit documents
, and performing related administrative tasks. A minimum of two years of research assistant experience is required to effectively complement and support the existing team. This is a priority hire
.

• Assist in the design, planning, and execution of clinical trials in accordance with study protocols.
• Collect, analyze, and interpret data from experiments and clinical studies with accuracy and attention to detail.
• Maintain comprehensive and accurate research records, logs, and documentation.
• Collaborate with research coordinators and investigators in preparing reports, charts, and presentations.
• Support laboratory tasks, including tissue and cell culture, assays, and sample handling.
• Ensure compliance with FDA regulations, GCP guidelines, and institutional SOPs.
• Prepare study-related materials and coordinate subject visits as needed.
• Manage appointment scheduling, patient recruitment efforts, incoming patient calls, and administrative tasks.

• Bachelor’s degree in Biology, Life Sciences, Biochemistry, or related field.
• Minimum two years of experience as a Research Assistant (required).
• Prior experience in clinical trials, biomedical research, or laboratory work (preferred).
• Strong understanding of molecular biology and cell biology principles.
• Familiarity with FDA regulations and ICH-GCP guidelines.
• Proficiency in Microsoft Office; experience with data analysis software (SAS, R, Python) is a plus.
• Excellent communication, time management, and organizational skills.
• High level of accuracy and attention to detail.