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Clinical Research Coordinator

System One

Las Vegas, NVContract$30/hrSeen 3w agoSeen in employer's feed 1 day ago

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At a glance

Compensation
$30/hr
Location
Las Vegas, NV
Schedule
Contract
Work Authorization
Not specified

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Job overview

The Clinical Research Coordinator will assist in coordinating and executing clinical research protocols, conduct screening visits, manage informed consent and enrollment, schedule study activities, collect and maintain data, communicate with participants, monitor study progress, adhere to SOPs and GCP guidelines, and handle specimen processing and documentation.

Skills & qualifications

RequiredNice to have

Skills

Basic Knowledge of Clinical ResearchMedical Terminology and Patient Care ExperienceStrong Organizational SkillsTime ManagementAttention to DetailClear CommunicationCollaborative TeamworkKnowledge of GCP, HIPAA, ALCOA, FDA Regulations, IATA GuidelinesExperience With Participant Screening and Informed Consent ProcessProficiency With Electronic Data Capture SystemsProficiency With Clinical Trial Management SoftwareMicrosoft Office ExcelMicrosoft Office WordMicrosoft Office PowerPointSpecimen Handling and ProcessingCritical Thinking

Qualifications

High School Diploma or EquivalentAssociate’s Degree or Higher in Health-Related FieldMedical Assistant CertificationCPR/BLS CertificationClinical Research Coordinator Certification

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match

Full 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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Ref: #568-Clinical

System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services 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 full-time 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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