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Temporary Field Research Jobs in Nevada (NOW HIRING)

Field Engineer

Reno, NV · On-site

$55K - $75K/yr

Designs temporary structures used during construction with emphasis on safety considerations ... Conducts research and accurately reports on project status * Performs quality control inspections ...

Field Engineer

Carlin, NV · On-site

$55K - $75K/yr

Designs temporary structures used during construction with emphasis on safety considerations ... Conducts research and accurately reports on project status * Performs quality control inspections ...

Field Engineer

Las Vegas, NV · On-site

$55K - $75K/yr

Designs temporary structures used during construction with emphasis on safety considerations ... Conducts research and accurately reports on project status * Performs quality control inspections ...

Field Engineer

Sparks, NV · On-site

$55K - $75K/yr

Designs temporary structures used during construction with emphasis on safety considerations ... Conducts research and accurately reports on project status * Performs quality control inspections ...

Designs temporary structures used during construction with emphasis on safety considerations ... Conducts research and accurately reports on project status * Performs quality control inspections ...

Office Assistant

Las Vegas, NV · On-site

$17 - $20/hr

Research, locate, and respond to various customer and associate inquiries. * Support Construction ... Maintain daily updates of all in-house field tickets with relevance to Temporary Meters.

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Showing results 1-20

Temporary Field Research information

What is the difference between Temporary Field Research vs Field Research Assistant?

AspectTemporary Field ResearchField Research Assistant
CredentialsTypically requires a relevant degree or experience in research methodsOften requires a related degree or coursework in research or social sciences
Work EnvironmentField sites, outdoor or remote locations, short-term projectsField sites, labs, or office settings, supporting ongoing projects
Employer & IndustryResearch firms, NGOs, government agencies, environmental organizationsUniversities, research institutions, NGOs, government agencies
Search & Comparison IntentUnderstanding short-term research roles, project-based workSupporting research projects, entry-level research roles

Temporary Field Research involves short-term, project-based work often in outdoor or remote locations, requiring relevant research experience or credentials. Field Research Assistants typically support ongoing research projects in various settings, often as entry-level roles. Both roles are common in research-focused industries but differ mainly in duration, scope, and level of responsibility.

What are the most commonly searched types of Field Research jobs in Nevada?

The most popular types of Field Research jobs in Nevada are:

What are popular job titles related to Temporary Field Research jobs in Nevada?

For Temporary Field Research jobs in Nevada, the most frequently searched job titles are:

What cities in Nevada are hiring for Temporary Field Research jobs?

Cities in Nevada with the most Temporary Field Research job openings:

Infographic showing various Temporary Field Research job openings in Nevada as of July 2026, with employment types broken down into 43% Full Time, 43% Part Time, and 14% Temporary. Highlights an 100% In-person job distribution.

Clinical Research Coordinator I

Las Vegas, NV

$29/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 29 days ago


Job description

Clinical Research Coordinator I
  • Location: Las Vegas, NV 89109
  • Schedule: Monday – Friday, 8:00 AM – 5:00 PM
  • Employment Type: Temp-to-Hire
  • Pay Rate: $29.00 per hour
Job Summary
We are seeking a dedicated Clinical Research Coordinator to support the 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, you will assist with patient screening, data collection, and the coordination of study activities to ensure accuracy, efficiency, and high-quality research outcomes. Note: Medical Assistants with strong direct patient care experience, as well as candidates with prior Research Assistant or lab coordination backgrounds, are strongly encouraged to apply.
Key Responsibilities
  • Participant Management: Conduct screening visits, collect medical history and basic vitals, and assist with the informed consent process and participant enrollment.
  • Study Coordination: Coordinate and schedule study visits, procedures, and follow-up activities; communicate with participants to provide education, answer questions, and support study adherence.
  • Data & Documentation: Collect, record, and maintain accurate clinical research data, source documentation, and medical history documentation. Perform data entry and scan, upload, and file organized study records.
  • Safety & Compliance: Monitor study progress, ask about and report any Adverse Events (AEs) or Serious Adverse Events (SAEs) during patient questionnaires, and adhere to site Standard Operating Procedures (SOPs) and Good Clinical Practice (GCP) guidelines.
  • Laboratory Support: Draw, process, and ship laboratory specimens (including the handling of dangerous goods) in accordance with regulations, if qualified.
  • Collaboration: Apply critical thinking skills to support efficient study operations, problem resolution, and transparent communication across fast-paced clinical teams.
Qualifications & Requirements
  • Education: High school diploma or equivalent required; an associate's degree or higher in a health-related field preferred.
  • Experience: Basic knowledge of clinical research strongly preferred. Direct patient care experience required (Medical Assistants, Research Assistants, or Lab Coordinators thrive well in this position).
  • Core Skills: Strong medical terminology knowledge, excellent organizational and time-management skills, high attention to detail, and the ability to communicate clearly and professionally with diverse populations.
  • Technical Knowledge: Familiarity with clinical research protocols, electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, PowerPoint).
  • Regulations: Knowledge of GCP, HIPAA, ALCOA principles, FDA regulations, and IATA guidelines strongly preferred.
Certificates, Licenses, and Registrations
  • 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

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