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Responsibilities

  • Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -
  • Responsible for all aspects of site management as prescribed in the project plans
  • General On-Site Monitoring
  • Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
  • Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
  • Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data
  • Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested
  • Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs
  • Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management
  • Assist with training of new employees, eg. co-monitoring
  • Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned
  • Perform other duties as assigned by management

Qualifications

  • Our FSP team is currently seeking a CRA 2 with 2 years of monitoring!
  • Seeking candidates in the Las Vegas, NV area with Oncology
  • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
  • 2 years of Clinical Monitoring experience

Required skills

Clinical MonitoringOncology

Full job description

FSP Clinical Research Associate 2 - Las Vegas, NV - Oncology jobs in United States

Fortrea

  • $100K/yr - $112K/yr
  • Biotechnology

Responsibilities

  • Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -
  • Responsible for all aspects of site management as prescribed in the project plans
  • General On-Site Monitoring
  • Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
  • Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
  • Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data
  • Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested
  • Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs
  • Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management
  • Assist with training of new employees, eg. co-monitoring
  • Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned
  • Perform other duties as assigned by management

Benefits

  • Remote role with 8–10 days on site per month, a mix of onsite and remote.
  • Fortrea is a provider of comprehensive Phase I through IV clinical trial management, clinical pharmacology, patient access solutions.
  • Durham, North Carolina, USA
  • https://www.fortrea.com
  • Distribution of Different Job Fields Receiving Sponsorship
  • Represents job field similar to this job
  • Engineering and Development
  • Management and Executive
  • Customer Service and Support
  • Sales
  • Legal and Compliance
  • Trends of Total Sponsorships
  • *2026
  • (21)
  • 2025
  • (14)
  • 2024
  • (25)
  • 2023
  • (6)
  • Late Stage
  • Leadership Team
  • Anshul Thakral
  • Chief Executive Officer
  • Agnieszka Gallagher
  • General Counsel, Chief Compliance Officer and Corporate Secretary
  • Recent News
  • TradingView
  • Fortrea Completes Acquisition Of The Early Phase Services Division From Worldwide Clinical Trials

Qualifications

  • Our FSP team is currently seeking a CRA 2 with 2 years of monitoring!
  • Seeking candidates in the Las Vegas, NV area with Oncology
  • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
  • 2 years of Clinical Monitoring experience

Required skills

  • Clinical Monitoring, Oncology

Experience

  • 2+ years

Job details

Employment type

Full-time

Seniority level

2+ years

Date posted

Oct 15, 2026

Work mode

Remote

Job source

fortrea.wd1.myworkdayjobs.com

Company

  • Remote, USA
  • Healthcare

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