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

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  • Elite Clinical Network
  • North Las Vegas, NV

Job Description

Position Summary

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.

This individual will also 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 .

Key Responsibilities

  • 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.

Required Qualifications

  • 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.

Job Tags

Work at office,

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