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  • Part-Time Clinical Research Coordinator

    Actalent (Las Vegas, NV)



    Apply Now

    Job Title: Clinical Research Coordinator (Las Vegas) - Part-Time

    Job Description

    The Research Coordinator will assist an Investigator, Research Associate, or Project Manager in operationalizing tasks associated with implementing a research study. This includes responsibilities related to recruitment, data collection, data management, and reporting of results.

    Responsibilities

    + Recruit and consent research participants.

    + Conduct telephone or in-person interviews with participants, including screening for eligibility.

    + Perform follow-up with study participants via telephone, e-mail, and/or mail.

    + Prepare, mail, and process questionnaires and other study correspondence.

    + Assist in tracking study participants using MS Excel.

    + Maintain accurate and detailed records and files of work.

    + Review, edit, clean, and enter participant data into a database.

    + Assist with literature reviews for proposal submissions and manuscript preparation.

    + Handle bookkeeping related to study budgets, including ordering supplies and requesting checks for payment and participant incentives.

    + Perform miscellaneous administrative tasks such as typing labels, copying, faxing, meeting preparation, note-taking, and transcribing audio files.

    Essential Skills

    + High school diploma or General Education Development (GED).

    + 3+ years of on-site hands-on Clinical Research Coordinator experience.

    + Experience in phlebotomy.

    + Proficiency in chart review, patient recruitment, electronic data capture (EDC), and electronic medical records (EMR).

    + Knowledge of clinical research and Good Clinical Practice (GCP).

     

    Additional Skills & Qualifications

     

    + Ability to quickly adapt and work independently.

    + Willingness and capability to train junior Clinical Research Coordinators at the site.

    Work Environment

    This is an on-site position within a clinic environment. The role requires 20 hours per week for the first three months, followed by 12-15 hours per week for another three months, with potential for extension. You will have the opportunity to work with one of the leading healthcare providers in the U.S. and engage in clinical research trials.

     

    Job Type & Location

     

    This is a Contract position based out of Las Vegas, NV.

    Pay and Benefits

    The pay range for this position is $30.00 - $45.00/hr.

     

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

     

    Workplace Type

     

    This is a fully onsite position in Las Vegas,NV.

     

    Application Deadline

     

    This position is anticipated to close on Jan 26, 2026.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

     

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

     

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.

     


    Apply Now



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