Assistant Clinical Research Coordinator

ALLIANCE CLINICAL LLC•Las Vegas, NV

4h•Onsite

About The Position

The Assistant Clinical Research Coordinator (ACRC) supports the planning, coordination, and execution of clinical research studies within a healthcare setting. This role ensures clinical trials are conducted in compliance with study protocols, regulatory requirements, and institutional policies while protecting participant safety and data integrity. Working closely with Principal Investigators (PIs), research staff, and study participants, the ACRC assists with participant screening, data collection, and the coordination of study activities to ensure accuracy, efficiency, and high-quality research outcomes. The company is dedicated to advancing medical innovation and healing technology through groundbreaking research, diligent patient care, and strong executive management. Their hands-on management team and medical staff are committed to rapid, efficient trials that bring life-changing drugs to market faster. The research staff brings years of experience conducting Phase 1-4 clinical studies, all dedicated to curing disease and improving individual quality of life. The mission of Alliance Clinical Network is to advance medical research by enrolling diverse populations in high-quality clinical trials, maintaining the highest standards of integrity and excellence, and ensuring every participant receives respectful and compassionate care. They strive to build a tightly knit, supportive, and collaborative environment where team members can thrive and make meaningful contributions to human health.

Requirements

High school diploma or equivalent required
Basic knowledge of clinical research principles, medical terminology, and healthcare environments
Strong organizational, time management, and attention-to-detail skills with the ability to manage multiple priorities
Ability to communicate clearly and professionally with diverse populations
Ability to work collaboratively in a fast-paced, team-oriented environment

Nice To Haves

An associate’s degree or higher in a health-related field
Experience in clinical research or healthcare settings
Knowledge of GCP, HIPAA, ALCOA principles, FDA regulations, and IATA guidelines
Experience with participant recruitment, screening, and the informed consent process
Proficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint)
Medical Assistant (MA) certification
Current CPR/BLS certification
Certification as a Clinical Research Coordinator (e.g., CCRC) or a willingness to obtain certification

Responsibilities

Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff.
Recruit, screen, and enroll study participants in accordance with protocol requirements and ethical guidelines.
Coordinate and schedule study visits, procedures, and follow-up activities with study participants and clinical teams.
Collect, record, and maintain accurate clinical research data and source documentation in compliance with regulatory and institutional standards.
Communicate with study participants to provide education, answer questions, and support adherence to study requirements.
Monitor study progress and report adverse events, protocol deviations, and other study-related issues to the research team.
Support the preparation, maintenance, and submission of regulatory documents; assist with audits and inspections as needed.
Adhere to site standard operating procedures (SOPs) and Good Clinical Practice (GCP) guidelines.
Perform front desk receptionist and administrative responsibilities as assigned.
Draw, process, and ship laboratory specimens, including the handling of dangerous goods, in accordance with regulations.
Scan, upload, file, and maintain organized study records and documentation.
Apply critical thinking skills to support efficient study operations and problem resolution.
Perform other duties as assigned.