Clinical Research Coordinator

System One; Las Vegas (NV); On-site; USD 39,000 - 44,000; Full time

Benefits offered by this job

Health and welfare benefits

401(k) plan

Job summary

System One is seeking a Clinical Research Coordinator in Las Vegas for a contract position onsite. The role involves coordinating clinical research protocols under the PI and senior staff, screening participants, and assisting with informed consent and enrollment.

You will schedule visits, collect and maintain data, communicate with participants, monitor progress, and ensure adherence to SOPs and GCP. Medical terminology knowledge and MA certification are preferred, with strong organizational

Qualifications

• High school diploma or equivalent required.
• Associate degree or higher in health-related field preferred.

Responsibilities

• Coordinate clinical research protocols under PI supervision.
• Screen participants and collect medical history.
• Assist with informed consent and enrollment of participants per protocol.
• Schedule visits and procedures with clinical teams.
• Maintain accurate data and documentation per GCP.
• Monitor progress and report adverse events.

Skills

Organizational skills

Communication skills

Attention to detail

Education

Associate degree or higher in health-related field

Job description

Job Title: Clinical Research Coordinator
Location: Las Vegas, NV
Type: Contract
Compensation: $30.00/hr
Work Model: Onsite
Hours: 40 hours

Responsibilities

• Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff.
• Conduct screening visits to collect medical history & other information from study participants.
• Assist with informed consent and enrollment of 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.
• Adhere to site standard operating procedures (SOPs) and Good Clinical Practice (GCP) guidelines.
• Draw, process, and ship laboratory specimens, including the handling of dangerous goods, in accordance with regulations (if qualified.)
• 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.

Requirements

• High school diploma or equivalent required; an associate’s degree or higher in a health-related field preferred.
• Basic knowledge of clinical research strongly preferred.
• Medical terminology & patient care experience required.
• 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.
• Knowledge of GCP, HIPAA, ALCOA principles, FDA regulations, and IATA guidelines strongly preferred.
• Experience with participant screening and the informed consent process strongly preferred.
• Proficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint) preferred.
• Medical Assistant (MA) certification preferred, Current CPR/BLS certification preferred, Certification as a Clinical Research Coordinator (e.g., CCRC) or a willingness to obtain certification preferred.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
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