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Temporary Clinical Research Informatics Jobs in Nevada

Zimmer Biomet

$14.75 - $19.50/hr

... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...

Zimmer Biomet

$14.25 - $19/hr

... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...

Zimmer Biomet

$15.25 - $20.50/hr

... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...

Zimmer Biomet

$14 - $18.75/hr

... in clinical research, primarily the Clinical Trial Management System (CTMS). How You'll Create ... Pursuing a bachelor's degree in Computer Science, Information Systems, Health Informatics, Data ...

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Temporary Clinical Research Informatics information

What is the difference between Temporary Clinical Research Informatics vs Clinical Data Coordinator?

AspectTemporary Clinical Research InformaticsClinical Data Coordinator
CredentialsTypically requires a degree in health informatics, life sciences, or related field; certifications like CCRA or CDMP are commonUsually requires a degree in health sciences or related field; certifications like CDMP may be preferred
Work EnvironmentWorks in clinical research settings, hospitals, or research organizations focusing on data management and informatics systemsWorks in clinical trial sites or research organizations managing data collection and entry
Employer & Industry UsageUsed by research institutions, pharmaceutical companies, and healthcare providers involved in clinical trialsCommonly employed by research sites, hospitals, and CROs managing clinical trial data

Temporary Clinical Research Informatics professionals focus on managing and analyzing clinical data using informatics tools, while Clinical Data Coordinators primarily handle data entry and quality control. Both roles are essential in clinical research but differ in scope and technical expertise.

What are the most commonly searched types of Clinical Research Informatics jobs in Nevada? The most popular types of Clinical Research Informatics jobs in Nevada are:
What cities in Nevada are hiring for Temporary Clinical Research Informatics jobs? Cities in Nevada with the most Temporary Clinical Research Informatics job openings:
Temporary Clinical Research Informatics jobs near you

Clinical Research Coordinator

ALLIANCE CLINICAL LLC

Las Vegas, NV • On-site

$23.25 - $30.75/hr

Temporary

Posted 5 days ago

Job description

*This is a full-time, temporary position currently estimated to last until December 31, 2026 (subject to business needs). There may be the possibility for this position to become permanent.*


Summary:

The Clinical Research Coordinator (CRC) supports 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, the CRC assists with participant screening, data collection, and the coordination of study activities to ensure accuracy, efficiency, and high-quality research outcomes.


Essential Duties and 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

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


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


ACN does not provide visa sponsorship for this role. Candidates who will require immigration or visa sponsorship at any time now or in the future (including, but not limited to, H‑1B, TN, or STEM OPT training plans) are not eligible for this role.


About the Company:

At Alliance Clinical Network, our mission is to advance medical research by enrolling diverse populations in high-quality clinical trials. We are committed to maintaining the highest standards of integrity and excellence, and to ensuring that every participant receives respectful and compassionate care. We strive to build a tightly knit, supportive and collaborative environment where our team members can thrive and make meaningful contributions to human health.