Contract Clinical Research Coordinator - Onsite, Las Vegas

Joulé; Las Vegas (NV); On-site; USD 39,000 - 44,000; Part time

Job summary

Joulé is seeking a Clinical Research Coordinator in Las Vegas, NV for a contract, onsite position. You will assist in coordinating clinical research protocols under PI supervision and ensure timely study activities.

The role requires a high school diploma (associate degree preferred), knowledge of clinical research, medical terminology, and strong organizational skills. Experience with informed consent, screening, data capture, and regulatory standards is desirable.

Qualifications

• 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 willingness to obtain certification preferred.

Responsibilities

• Assist in coordination and execution of clinical research protocols.
• Screen visits to collect medical history and information from study participants.
• Assist with informed consent and enrollment of study participants.
• Coordinate and schedule study visits, procedures, and follow-up activities.
• Collect, record, and maintain accurate clinical research data and source documentation.
• Communicate with study participants to provide education and support adherence.
• Monitor study progress and report adverse events, protocol deviations, and other issues.
• Adhere to site SOPs and Good Clinical Practice guidelines.
• Draw, process, and ship laboratory specimens (if qualified).
• Scan, upload, file, and maintain organized study records.
• Apply critical thinking to support efficient study operations.
• Perform other duties as assigned.

Skills

Medical terminology

Patient care

Communication

Organizational skills

Time management

Attention to detail

Teamwork

Microsoft Office

EDC experience

Excel

Education

High school diploma

Associate degree in health-related field

Tools

EDC systems

CTMS

Microsoft Excel

Word

PowerPoint

Job description

Joulé is seeking a Clinical Research Coordinator in Las Vegas, NV for a contract, onsite position. You will assist in coordinating clinical research protocols under PI supervision and ensure timely study activities.

The role requires a high school diploma (associate degree preferred), knowledge of clinical research, medical terminology, and strong organizational skills. Experience with informed consent, screening, data capture, and regulatory standards is desirable.